Day: October 25, 2018

Notice of the State Drug Administration on the suspension and rectification of Tianjin Vivadentai Biotechnology Co., Ltd. (No. 104 of 2018) Recently，The State Drug Administration organized an unannounced inspection of Tianjin Vivadentai Biotechnology Co., Ltd。Checking，The following deficiencies were found in the company's quality management system： One、In terms of organization and personnel, the company appointed a management representative on May 1, 2017，However, the actual work is sales and research and development，The company has not taken steps to raise awareness among employees of the requirements of the quality management system，It does not comply with the "Good Manufacturing Practice for Medical Devices" (hereinafter referred to as the "Specification") in which the management representative is responsible for the establishment、Implement and maintain a quality management system，Report on the operation of the quality management system and the need for improvement，Improve employee compliance with regulations、Requirements for the awareness of regulations and customer requirements。 Two、In terms of equipment, the company is not equipped with equipment to detect X-ray blocking items，Testing has not been commissioned，Enterprises that do not comply with the "Specification" shall be equipped with inspection instruments and equipment that are compatible with the product inspection requirements，The main inspection instruments and equipment shall have clear requirements for operating procedures。 Three、In terms of design and development, the output data of the company's product design and development does not include the product formula，The following performance index requirements in the product technical requirements are not included：X-ray blocking、Tensile bond strength、Shear bond strength、Composition and percentage，The design and development output of enterprises that do not comply with the "Specification" shall meet the input requirements，Procurement is included、Information required for production and service、requirements for product technical requirements, etc。 Four、Production management (1) Enterprise process flow chart (SC-SOP-01，Edition B/2017) stipulates the process as follows:：Raw material procurement, inspection, material breaking, lathe processing, polishing, curing, cleaning, inspection, packaging, warehousing，The company changed the actual production process to lathe processing - material breaking，Failure to compile material cutting process regulations and work instructions，Spot check production records (JL-7.5-03, fiberglass piles，Specification and model VIVAdental-V3, production batch number 180608) changed the production process as:：Wash - cure，Enterprises that do not comply with the "Specification" shall prepare production process regulations、Work instructions, etc，Clarify the requirements of key processes and special processes。 (2) Spot check the production records of enterprises (JL-7.5-03，Fiberglass piles，Specification model VIVAdental-V3, production lot number 180608)，The batch quantity is not recorded、Process parameters、Main equipment，Each batch (Taiwan) of products that do not comply with the "Specification" shall have production records，and meet the requirements of traceability。 Five、In terms of quality control, the following performance indicators in the registered product technical requirements are not covered by the company's product inspection procedures：Flexural performance、Flexural modulus of elasticity、X-ray blocking properties、Tensile bond strength、Shear bond strength、Composition and percentage，Enterprises that do not comply with the "Specification" shall formulate product inspection procedures according to the mandatory standards and the technical requirements of the products that have been registered or recorded，And the requirements for issuing corresponding inspection reports or certificates。 Tianjin Vivadentai Biotechnology Co., Ltd. has confirmed the deficiencies in its quality management system。The above behavior of the enterprise did not comply with the relevant provisions of the Good Manufacturing Practice for Medical Devices，There are serious deficiencies in the production quality management system，The State Drug Administration instructed the Tianjin Municipal Commission for Market and Quality Supervision to order the enterprise to immediately suspend production for rectification in accordance with the law，For those involved in violation of the Regulations on the Supervision and Administration of Medical Devices (Order No. 680 of the State Council) and relevant laws and regulations，Handle it seriously in accordance with the law。At the same time, the Tianjin Municipal Market and Quality Supervision and Administration Commission was instructed to require the enterprise to assess product safety risks，It may lead to potential safety hazards，It should be in accordance with the provisions of the "Administrative Measures for the Recall of Medical Devices" (Order No. 29 of the State Food and Drug Administration).，Product recall。 Production can only be resumed after the enterprise completes all project rectification and is qualified by the Tianjin Market and Quality Supervision and Administration Commission。 Notice is hereby given。 State Food and Drug Administration October 18, 2018 Notice of the State Drug Administration on the Suspension of Production and Rectification of Nanjing Yigao Microwave System Engineering Co., Ltd. (No. 105 of 2018) Recently，The State Drug Administration organized an unannounced inspection of Nanjing Yigao Microwave System Engineering Co., Ltd。Checking，The following deficiencies were found in the company's quality management system： One、In terms of equipment, material weighing is not equipped with suitable weighing equipment，Such as in warehouse 1，The transformer material is placed in a dense manner without packaging，Some of the transformer insulation was scratched，Detection of the number of stainless steel bars in and out of the warehouse，Managers say that the weighing method is used to determine this，During verification, it was found that the stainless steel strip was sagging to the ground，Cannot be weighed accurately，Enterprises that do not comply with the "Good Manufacturing Practice for Medical Devices" (hereinafter referred to as the "Specification") shall be equipped with appropriate measuring instruments，The measuring range and accuracy of the measuring instrument shall meet the requirements of use，Measuring instruments shall be marked with the validity period of their calibration，Requirements for keeping appropriate records。 Two、In terms of design and development, the power output of the bipolar coagulation mode of the high-frequency surgical system of the enterprise has changed from 0-120W to 0-80W，Failure to provide confirmed design change materials，It does not meet the requirements of the Code that enterprises should identify and keep records of changes in design and development。 Three、Production management: On-site verification of high-frequency electrosurgical unit (No. 16121506)，The company failed to provide relevant production inspection records，Not traceable，Each batch (Taiwan) of products that do not comply with the "Specification" shall have production records，and meet the requirements of traceability。 Four、In terms of quality control, the company failed to formulate factory inspection procedures and inspections in strict accordance with the national mandatory standards，GB9706.4 requires a high-frequency leakage current to test the load resistance of 200 ohms，Test resistance 200 ohms，Line spacing 50cm，The load resistance for the operator is 400 ohms，Test resistance 200 ohms，Line spacing 25cm for testing，Spot check cable withstand voltage test during the production process，The operating procedure requires 10s to 1000V，Hold for 1min；Actually 20s to 1000V，Keep it for 40s，In the finished product inspection，The high-frequency leakage current test requires 10s to 1000V，Hold for 1min，Actually in 18s it rises to 4000V，Hold for 42s，Enterprises that do not comply with the "Specification" shall formulate product inspection procedures according to the mandatory standards and the technical requirements of the products that have been registered or recorded，And the requirements for issuing the corresponding inspection report or certificate。 Nanjing Yigao Microwave System Engineering Co., Ltd. has confirmed the defects in its quality management system。The above behavior of the enterprise did not comply with the relevant provisions of the Good Manufacturing Practice for Medical Devices，There are serious deficiencies in the production quality management system，The State Drug Administration instructed the Jiangsu Provincial Food and Drug Administration to order the enterprise to immediately stop production and rectify in accordance with the law，For those involved in violation of the Regulations on the Supervision and Administration of Medical Devices (Order No. 680 of the State Council) and relevant laws and regulations，Handle it seriously in accordance with the law。At the same time, the Jiangsu Provincial Food and Drug Administration was instructed to require the company to assess product safety risks，It may lead to potential safety hazards，It should be in accordance with the provisions of the "Administrative Measures for the Recall of Medical Devices" (Order No. 29 of the State Food and Drug Administration).，Product recall。 Production can only be resumed after the enterprise completes all project rectification and is qualified by the Jiangsu Provincial Food and Drug Administration。 Notice is hereby given。 NMPA October 18, 2018

GB/T 19001-2016/ISO 9001：2015"Quality Management System Requirements" since its issuance，For new additions and changes to the standard，Each certification body organizes discussions with relevant professionals，At the same time, the content of the original standard is compared，to enhance understanding and unify understanding。Here, the author focuses on GB/T 19001-2016/ISO 9001：2015Standard 8.5.1f) "When the output cannot be verified by subsequent monitoring or measurement."，Confirm and periodically reconfirm the ability to realize the process planning of product and service provision".，This process is often referred to as a special process。 For every production enterprise，Planning and control processes in operation，should be recognized、Determine the special processes in the production process。Because special processes are the key processes that affect the intrinsic quality characteristics of the product，Hence how to control the special process，Whether or not to confirm the process capability，How to confirm the process capability，and the timing of confirmation、methods, etc，Affects the ability of process results to meet requirements，It plays an important role in achieving product quality goals。This article is based on this background，This paper attempts to explore the role of certification audit in improving the performance of process management。 Related theories and literature review certification audit "Certification and Accreditation Regulations" pointed out，Certification is the certification of an organization's products by a nationally recognized certification body、serve、The management system complies with the relevant technical specifications、Conformity assessment activities of mandatory requirements or standards of relevant technical specifications。 Audit (GB/T 19000-2016 in 3.13.1)，A system to obtain audit evidence and conduct an objective evaluation to determine the extent to which audit criteria are met、Independent、The process of forming a document。 Accreditation is based on standards and technical specifications，Help enterprises to establish a quality management system for sustainable improvement，And through the transmission of trust mechanism, guide all parties in society to participate in quality co-governance，For products that improve at the micro level、serve、The quality of the project and even the quality of economic development at the macro level，All of them play a role in basic guarantee and leading promotion。 Special Process Special Process (GB/T 19000-2008 4.1 Note 3)：The process of verifying whether a product is qualified or unsatisfactory or uneconomically。 Special Procedures (GJB 1405A-2006 in 4.2)：Intuitive and not easy to spot、The process by which the intrinsic quality characteristics of a product are formed that are not easily or economically measurable。Chemistry is often included、metallurgy、creature、optics、electronic and other processes。In machining，The common ones are casting、forging、weld、Surface treatment、heat treatment, etc。 It can be seen from this，Special processes are inherent。During the implementation of special processes，The intrinsic quality characteristics of the product have changed。Company H as an example in this article is an aluminum alloy profile processing enterprise，Determine "aging processing" as a special process，The author found in combination with the on-site audit，Explain the impact of product quality caused by the uncontrolled process of special processes，Further clarify the importance of certification audits in facilitating enterprise process management、The role of improving process management performance。 Process Management Performance Process management refers to:：Use a set of practical methods、technology and tools to curate、Control and improve the effectiveness of the process、Efficiency and adaptability，Including process planning、Process implementation、There are four parts: process monitoring (inspection) and process improvement (disposal).，That is, the PDCA cycle has four stages。The PDCA cycle is also known as the Deming cycle，It was put forward by Deming, a master of quality management, on the basis of Sheukhart's idea of statistical process control。 The ISO 9001 standard proposes a process-based quality management system，Continuous improvement of the quality management system through the four stages of the PDCA cycle。This paper mainly discusses the special processes involved in the production of enterprises，Further focus on the significant impact of special process management on product quality characteristics，to analyze how enterprises can make good use of GB/T 19001-2016/ISO 9001：2015standard，Identified in accordance with the requirements of 8.5.1f、Confirm the special process，Confirmation of the ability of the special process to meet the requirements，and carry out effective control，Promote the improvement of process management performance。 Performance (GB/T 19000-2016 3.7.8)，Measurable results，Quantitative or qualitative results may be involved。Performance is an indicator that reflects the effectiveness and effectiveness of an organization's operations，It can be measured by a set of indicators，It is influenced by different research objects and different research angles，Scholars also differ in their definitions of organizational performance，But scholars generally agree on one view，It's that performance is a composition, not just a concept。 Peter S. F. Drucker thinks，Effectiveness refers to the ability to do the right thing，That is, setting an appropriate goal and achieving that goal。 Process management performance，It is a combination of a set of evaluation process indicators，It is used to measure the quality of enterprise process control results。In this paper, the classification of process management performance evaluation indicators is mainly process indicators and quality indicators。 Certification audit theory basis standard Understand the requirements of GB/T 19001-2016 standard 8.5.1f) GB/T 19001-2016 standard 8.5.1 control of production and service provision，It is based on GB/T 19001-2008 standard 7.5.1 "Production and service provision process control" and 7.5.2 "Confirmation of production and service provision process".，The requirements have been consolidated and expanded。From the structural design of the standard clauses，GB/T 19001-2016 will be the 2008 version of the standard 7.5.1、7.5.2The Terms are consolidated into Clause 8.5.1，Requires organizations to set controls for product and service provision，combined with the nature of its products and services，Determine what controlled conditions are required in the production and service process，Plan and determine what specific controls to be in place。This clause gives controlled conditions in a) ~ h) 8 aspects，where f) "when the output cannot be verified by subsequent monitoring or measurement."，Confirm and periodically review the ability to plan the process of realizing product and service provision"，It is also one of the controlled conditions。Compared with the 2008 version of Standard 7.5.2，It is further emphasized that the process is an integral part of the production and service process，It is a key process that affects the intrinsic quality characteristics of the product，It is necessary to devise specific methods and measures to control them，And in the production process, the process capacity is confirmed and reconfirmed according to the planned arrangement。 GB/T 19001-2008 standard 7.5.2 audit practice The author combines years of audit practice and review of audit materials，It is calculated from the audit data information of 100 production enterprises，Clause 7.5.2 of GB/T 19001-2008 standard，50%of the production enterprises chose to delete，The reason is：The production process of the company's products can be verified by inspection，Processes that do not occur after the product has been used or the problem has become apparent after the service has been delivered。The other 50% did not delete the reviewee of the clause，While identifying and identifying the processes that need to be confirmed in the production process，Guidelines and methodologies for process capability validation are set out in the document，Required when the device、personnel、craft、When there is a change in any conditions such as materials，The process capability should be reconfirmed。But the audit found，80%The auditee above only provides a "Process Capability Qualification" table for the process to be validated at the time of initial certification，After that, the annual audit is "equipment."、personnel、craft、No change in material"，Evidence of process capability confirmation cannot be provided。However, in the actual production process，As customer requirements change、The need for quality upgrades or changes in suppliers，will cause the material、craft、equipment、Changes in any one or more of the personnel。Reasons for this result：First, enterprises do not understand the special process，At the time of quality management system planning，The methods and guidelines for confirming the capability of the process do not correspond to the actual characteristics of the product，Confirmation results do not confirm that the process capability meets the quality characteristics，Therefore, it is believed that "doing such evidence" is only for the purpose of certification，There is no practical point；Second, enterprises have their own methods for confirming process capabilities，Because of the lack of understanding of the requirements of the standard，Therefore, effective process validation is excluded from the management system，As a result, the certification audit cannot be obtained。visible，How can companies incorporate effective controls into their management systems，How can auditors collect effective evidence of enterprise process control during the audit process，It directly affects the awareness and trust of enterprises in certification audits，This affects the role of certification audit on the improvement of enterprise process management performance。 Certification Audit and Enterprise Process Management Performance Case Study GB/T19001-2016 Standard 8.5.1 Incorporates the processes that need to be confirmed into the control，First, inappropriate prunings were avoided，Second, the framework and requirements for identifying guidelines and methods have been removed，It is more conducive to the effective combination of the actual control of the production process and the application of standards。The following is a case study of Company H's 2015 surveillance audit，Take the audit found that the special process (timeliness treatment) control is not in compliance with the situation and rectification as an example，Analyze and discuss the role of certification audit in improving the performance of enterprise process management.。 Company Information Company H was established in May 2003，The registered capital is 100 million yuan，It is a private enterprise engaged in the processing of various aluminum alloy profiles。At present, the company has a total of 14 sets of 500T~2600T and continuous extruders and supporting electrophoresis、oxidation、Spraying (introduction of Gema in Switzerland)、Thermal insulation and energy-saving door and window profile composite production line、Several solar photovoltaic frame deep processing production lines and other supporting facilities，It is able to produce more than 300mm of external circles，An extra-long complex cross-sectional profile with an effective length of 14 meters。At present, the company has an annual output of 1060、6063、6005、6061、6082and other alloys, aluminum alloy profiles of more than 30,000 tons。From 2004 to 2005, the company completed the GB/T 19001 quality management system in two steps、GB/T 24001 Environmental Management System、GB/T 28001 Occupational Health and Safety Management System Certification。 Case Background The company's management manual identifies the determination of extrusion、aging、oxidation、spray coating、Electrophoresis is a special process。 20143 non-conformance reports were issued during the annual supervision and audit，Among them, "the No. 3 furnace on site is aging the product with the profile number TM079 of alloy 6005T5，The "Extrusion Process Operation Procedure" used in the workshop does not extrude the alloy grade、Specification of aging process parameters"，It does not meet the requirements of clause 7.5.1 of GB/T 19001-2008 standard。 20152 non-conformity reports were issued for annual supervision and audit，thereinto：The on-site aging furnace is being aged and kept warm for 6063T5 products，6The temperature of each area is displayed separately：158℃、172℃、183℃、174℃、193℃、188℃、216℃；4The insulation temperature of each zone does not meet the requirements of 190 °C ± 5 °C required by the "Extrusion Process Operation Regulations".，It also does not meet the requirements of clause 7.5.1 of GB/T 19001-2008 standard。 The above two audits found non-conformity，On the surface, the problem is different，It is not a product of the same grade，And one is process planning，One is process control，However, the essence is "aging treatment" process control，"Timeliness" is a special process，Changes that affect the intrinsic quality characteristics of the product。 Special Process Process Control Analysis Non-conforming materials submitted in 2014：Non-conformity cause analysis：The company does not have a good understanding of standard learning，The field is controlled by experience，Process parameters were not developed as required；Non-compliance with corrective actions：Modification of "Extrusion Process Operating Regulations"，Increase extrusion、Aging process parameters；The aging treatment, heating temperature and holding time are specified。 2015The year is the second supervision and audit of the quality management system，Combined with the first supervision and audit of the environmental and occupational health and safety management system，The audit team consists of team leaders, 4 auditors (1 of whom is an intern)，The level auditors are all professional auditors，Have professional audit capabilities，And the audit team leader has a basic understanding of the production process of the enterprise。2015On September 18, he had professional communication with the members of the group at the audit preparation meeting，At the same time, it is reminded that the audit process should focus on tracking the effectiveness of corrective actions that did not meet the requirements of the previous year：extrusion、Review and extrusion of suitability of aging process indicators、Aging process execution and control。 During the on-site audit，Professional auditors on the key processes of production：extrusion、aging、oxidation、spray coating、electrophoresis, etc，Sampling inspections were carried out according to the method of process audit，Relevant documents and records were consulted，And the focus is on extrusion、Process documentation for aging furnaces，The production workshop provides the "Extrusion Process Operating Regulations"，File to extrusion temperature、Transmission speed、The aging treatment, heating temperature and holding time are specified；Follow-up review and confirmation of the specified process parameters，The company offers a "squeeze."、Validation form of aging process"，Confirm that the device meets the requirements，Personnel are trained，Process stability"，For devices、personnel、What is the basis for the process to meet the requirements?，Unable to provide relevant evidentiary materials。The team leader communicated with the relevant person in charge of the enterprise，Understand the actual situation at which the process parameters were determined。According to the head of the enterprise：The temperature of the extrusion process of the aluminum alloy profile、Transmission speed，The temperature of each section of the aging furnace，Warming、The time to keep warm，The production team has been debugged many times，Finalized process specifications。The audit team also asked the production team to provide the temperature of the multiple commissioning processes、Recording of the time and hardness test results。For the site, no evidence was provided to the professional auditor，The squad leader explained，According to the different requirements of customers for product performance，Frequent adjustments to the production process，It's all recorded in a small notebook，Not controlled within the scope of the management system，What is controlled is the "squeezing."、Validation form of aging process"。 The results of the analysis can be seen，Enterprises because of the lack of understanding of the requirements of the standard，Exclude valid process capability validation from the management system。If the audit process cannot be tracked in depth and continuously，It will lead to the failure to collect evidence，The management system of certification audit and the actual process management of the enterprise are "two skins"，Helping companies establish a quality management system for sustainable improvement has become an empty phrase。 The audit team further observed the actual control of the process on site，It was found that the aging furnace was undergoing aging insulation of 6063T5 products，7The temperature of each area is displayed separately：158℃、172℃、183℃、174℃、193℃、188℃、216℃，The insulation temperature of 5 of the zones did not meet the requirements of 190°C ±5°C。The purpose of aging treatment of aluminum alloy profiles is to eliminate the internal stress of the workpiece，Stabilize tissue and size，improve mechanical properties, etc，Manual aging processing，The allowable deviation of the heating temperature of aluminum alloy solution treatment is only 5°C，So，Poor control may affect the quality of product performance。The audit team communicated with the supervisor of the auditee，A non-compliance report was issued for this。In the process of discussion and communication with management representatives，The two sides also held full discussions on this issue，Representatives of business managers recognized，Aging treatment of the heating process、Maintain temperature、Holding time is the main reason affecting the performance and quality of aluminum alloy profiles。 At the last meeting, the head of the audit team put forward requirements for non-compliance rectification，The difference between corrective and corrective actions is explained，Emphasis is placed on starting with "people."、machine、material、law、ring、and other aspects to analyze and find the cause of the temperature difference，Develop corrective actions for the cause，Ensure the effectiveness of improvements，It is also required to provide evidence of the hardness index inspection of the batch of products together with the rectification materials。 on this，The management representatives of the enterprise attach great importance to it，The production department is clearly required to organize the extrusion workshop，The quality inspection department cooperates with the cause analysis of the non-conformity，Implement corrections、Corrective Actions。On October 14, 2015, the company submitted a non-compliant closure material：The hardness test record of this batch of products，The results are qualified；Non-conformance rectification report。 Cause analysis：The production department organized personnel to inspect the aging furnace and the temperature gauge，Search through several aspects，Finally, it was found that the temperature display of 7 areas of the large aging furnace was inconsistent，The main reason is that there are 6 areas where the thermocouples are loose and not in place，This results in a discrepancy between the measured temperature and the actual temperature。 Corrective Actions：Production maintenance personnel repair thermocouples in all 7 areas，After resetting the thermocouple that is not in place，After many observations and data tracking，The actual temperature measured is consistent with the specified temperature of the process。 Verification of effectiveness：Display photo of the actual temperature measured during the heating process and holding process of aging furnace 6063T5 (October 14, 2015)；Tracking record of the data after the thermocouple reset of the aging furnace and evidence of passing the hardness test (tracking data from September 23 to September 28, 2015.)，and the test data on October 14)。 The results of the analysis can be seen，Enterprises should comply with GB/T 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ST Huifeng lost 340 million yuan in the third quarter、Net profit decreased by 462% year-on-year, and many of its subsidiaries stopped production due to environmental problems Beijing News Express(Reporter Li Yunqi)ST Huifeng(Former Huifeng shares)The announcement was made on October 24，to its coal-water slurry project assets、Huatong Chemical's productive fixed assets and projects under construction were respectively provided for impairment。The company's third-quarter report released at the same time shows，7-9Monthly ST Huifeng lost 340 million yuan，Net profit decreased by 462% year-on-year。 The first three quarters report shows:，7-9The monthly operating income of ST Huifeng was 690 million yuan，33.26% lower than the same period last year。1-9The monthly ST Huifeng operating income was 2.338 billion yuan。-16.96% lower than the same period last year。7-9month，ST Huifeng's net profit attributable to shareholders of listed companies was -340 million，462.23% lower than the same period last year。1-9Monthly net profit attributable to shareholders of listed companies - 244 million，-174.23% decrease from the same period last year。 Behind such performance，Since April this year, ST Huifeng's workshop has been shut down due to environmental protection issues、The company is under investigation、penalties and other events。 April 20 of this year，The Ministry of Ecology and Environment (MEE) has notified ST Huifeng in Yancheng City of its long-term illegal disposal and illegal storage of hazardous waste。20day of the day，ST Huifeng received a letter of concern from the Shenzhen Stock Exchange，Three days later, a notice of investigation was received from the SFC，Suspected of violating laws and regulations in information disclosure，ST Huifeng was investigated。According to ST Huifeng's announcement，In addition to the environmental protection workshop，Other production workshops are to be suspended for rectification。furthermore，On suspicion of the crime of polluting the environment，Directors of the Company、Deputy General Manager Ji Zihua was arrested on May 15。6month，The branch directly under the Yancheng Municipal Public Security Bureau filed a case for investigation of ST Huifeng for "suspected environmental pollution crimes".。 Factories in some of ST Huifeng's subsidiaries were also shut down。2018April 28，Three subsidiaries of ST Huifeng received the "Notice" from the People's Government of Guannan County，According to the spiritual requirements of the provincial and municipal governments on the rectification of outstanding environmental problems in the estuary，All enterprises in the park are required to carry out centralized rectification，Lianyungang Huatong Company、Jialong Chemical Company and Zhicheng Chemical Company entered into suspension of production and carried out self-inspection，Carry out rectification in a timely manner。 May 9, 2018，ST Huifeng's subsidiary, Jiangsu Kefit, received the "Penalty Decision" from the Dafeng District Environmental Protection Bureau，The company's environmental protection facilities shall not be resumed without environmental protection acceptance，The company implements suspension of production and rectification。 September 2018，ST Huifeng to the "Administrative Penalty Decision" issued by the Jiangsu Provincial Environmental Protection Department，The decision requires the company to organize the dismantling of the new high-concentration COD wastewater-to-coal slurry incineration by-product steam project(years of disposal 30000 tons of highly concentrated C0D wastewater)The use of coal-water slurry boilers。 9May 18th，Lianyungang Huatong Chemical, a subsidiary of ST Huifeng Holdings, received the "Administrative Penalty Decision" from Guannan County Environmental Protection Bureau，Order the business to close。 Subject to the above discontinuation、demolition and other impacts，ST Huifeng's coal-water slurry project assets、Huatong Chemical's productive fixed assets and projects under construction were respectively provided for impairment。 ST Huifeng said，As of September 30, 2018，The book value of the project under construction of ST Huifeng coal-water slurry project is 91.58 million yuan，The parent company made an impairment provision of 69.02 million yuan;The book value of fixed assets of Huatong Chemical is 367 million yuan，The book value of the project under construction is 21.08 million yuan，Huatong Chemical made an impairment provision of 94.46 million yuan for productive fixed assets and projects under construction;Huatong Chemical's net book assets were -680,000 yuan，The book value of the parent company's long-term equity investment in Huatong Chemical is 100 million yuan，The parent company made an impairment provision of 100 million yuan for long-term equity investment。 According to ST Huifeng's announcement，Its preparation workshop(J10、I10、I51)Production resumed on September 26, 2018，In 2017, the company's preparation business achieved revenue of 675 million yuan，28.2% of the parent company's revenue，"The company will strictly enforce safety、Relevant laws, regulations and standards in environmental protection，Further improve the level of internal cleaner production and continuous improvement"。 source：Beijing News statement：This number is reprinted、share、statement、Views remain neutral，The purpose is only to convey more information，The copyright belongs to the original author。If the copyright of the work is involved，Please contact us，We will remove the content as soon as possible!