Product Details
What information do I need to provide for D panel lamp certification? How much?
Hello dear customer:
I am Xiao Wu from Luxshare Laboratories. Our company is located in Bao’an District, Shenzhen City and has been established for several years. We have advantages in testing and certification
Company Certification includes. Europe: (:)r
. Asia:
. Australia:
. America: (:D)D
. Africa:
. Taobao/ Tmall Mall and other quality inspection reports
Thank you for taking time out of your busy schedule to take a look at your company. If necessary, please contact Xiao Wu
Mobile: We sincerely hope to cooperate with you!
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r .Application process
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r .Factory inspection
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r .First factory inspection< br/> .r
r .After accepting the product certification application, a first factory inspection of the factory is required to conduct a preliminary assessment of the factory's quality control system. According to the laws and regulations related to Korean safety certification and
r., factories should have the following documented procedures or regulations that are consistent with factory quality management and product quality control:
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r.Product change control procedures (for example: after the certification product change application is approved by the certification body, the corresponding technical documents should be formulated strictly in accordance with the approved changes and distributed to the relevant departments
r < br/>r. To correctly implement changes to certified products. Unapproved changes cannot impose certification marks on the changed products.
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r .Document and data control procedures
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r .Quality record control procedures (the retention period of incoming, routine and operational inspection records is at least
/>r .Year)
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r .Routine inspection and confirmation inspection procedures
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r .No Qualified product control procedures
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r . Inspection or verification procedures for key components and materials
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r . Internal quality audit procedures
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r . Process operation instructions, inspection standards, instrument and equipment operating procedures, management systems and other procedures. The factory should keep at least the above quality records to verify The factory has indeed carried out all production inspections and production tests. Quality records should be true and valid
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r. Product routine inspection and confirmation inspection records, incoming inspection of key components and materials
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r. Verification records and certificates of conformity provided by suppliers:
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r. Records of regular calibration or verification of inspection and testing equipment
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r .Routine inspection and confirmation (operation) inspection records
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r .Routine inspection records of safety equipment on the production line (workshop)
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r. Disposal records of non-conforming products (incoming, routine and operational)
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r. Records of internal audits
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r. Responsible for customer complaints Record of corrective actions taken
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r .Record of correction of non-conformities in operational inspection
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r .Annual factory inspection
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r. After the certificate is issued, the certification body will conduct an annual follow-up review of the factory every year. The purpose is to review whether the consistency of the factory's quality control system can continue to meet safety standards. The annual factory inspection is divided into two parts:
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r . The viewing requirements and content of quality documents, quality records, and production site related content are basically the same as the first inspection.
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r . Need to confirm the consistency of all factory products authorized with the
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r .mark. Confirm the key components,
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r materials, circuits, structures, etc. of the certified product according to the attached page of the product's authorization certificate (list of key components) to see if they are consistent.
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r .Sampling inspection
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r .Included within the scope of compulsory certification of the
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r .mark There are currently
r kinds of products. The Korean Safety Law stipulates that all types of products be sampled every year, so each product is sampled once a year. The sampling method is: carried out by factory inspectors during the annual inspection. When there is production or inventory on site, the inspector seals the factory
r. The samples will be sent to the designated location within three months. When the factory is inspected, when there is no production or inventory. The designated samples must be sent to the designated location within
r months.
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