CCS advantages of CCC services:
1. CCC factory inspection is another item that is easy to fail or non-compliance. So, what exactly is being checked? What are the relevant requirements? CCS professional team can guide you or your vendors cost and time saving.
Main contents of product certification factory inspection include the inspection of "factory quality assurance ability" and "product consistency". Enterprises applying for CCC certification should aim to ensure the consistency of the certified products and type test samples, establish the corresponding quality assurance capability according to the requirements of factory quality assurance capability and the requirements of the corresponding product certification implementation rules/rules, and in view of the product characteristics and production and processing characteristics.
2. Which departments and places should be inspected and which documents and records should be consulted during on-site inspection?
Generally speaking, the on-site inspection mainly involves the certification of product manufacturing and quality control related departments and sites; The main documents referred to in field inspection are technical documents and system management documents related to certified products; The main inspection records are related to the management records of certified products. This part is often found to be inconsistent with the project. CCS has a complete set of data system, and our counselors can guide and train the factory to improve it, so as to ensure one-time approval.
3. How many kinds of factory inspection conclusions are there?
Factory inspection results are usually divided into four types: "Factory inspection passed", "written verification passed", "site verification passed", "factory inspection failed". Among them, "written verification passed" refers to the existence of nonconformance, the factory carries out rectification within the prescribed time limit, the certification body carries out written verification of the relevant materials of the rectification measures, if valid, the factory inspection passes, otherwise it does not pass; "Site verification passed" means that there is a nonconformance, the factory carries out rectification within the specified period, the certification body carries out on-site verification of the rectification measures, if valid, the factory inspection passes, otherwise it does not pass. CCS 'professional rectification team will provide professional guidance for non-conforming projects to ensure that rectification measures are reasonable and approved.
4. What problems do the factory have that do not meet the requirements? How to rectify them?
In general, any failure to meet factory quality assurance capability requirements, product conformance requirements, product standards requirements or factory related management system documentation may result in non-compliance. The inspection team will issue a "nonconformance report" to inform the factory of the nonconformance problem. The non-conformance report will contain the description of the non-conformance problem, the judgment of the non-conformance terms, the rectification period and the content of the verification method. CCS training tutors can also provide pre-audit services (additional cost) so that there are no major inspection defects.
5. What problems will cause the factory to fail the inspection?
Common situations that lead to factory inspection failures are:
a. The specified test results are not qualified;
b. Key resources do not meet requirements.
c. There is a serious problem of product consistency, resulting in the product does not meet the standard requirements;
d. Obvious defects exist in the product, which may lead to quality and safety accidents;
e. Product consistency control requirements are not effectively implemented, resulting in product inconsistency and systematic failure of quality assurance capability; f. During the period of non-conformity, the factory fails to take corrective measures, fails to submit corrective information on time, or remains unqualified after rectification.
CCS training tutors can also provide pre-audit services (additional cost) so that there are no major inspection defects.
6. How should the rectification of non-conformity be implemented?
There are usually at least 5 steps:
a. Familiar with certification requirements;
b. Rectify any non-conformance that has occurred;
c. Analyze the causes of nonconformity;
d. Develop and implement corrective measures according to the causes;
e. Self-confirm that the above corrections and corrective actions are implemented in compliance with certification requirements.
7. What should I pay attention to when submitting rectification materials? When submitting rectification data to the inspection team, pay attention to:
a. The contents of cause analysis, correction and corrective action shall be described in the nonconformance report;
b. Evidence (documents, records, pictures, etc.) should be submitted to support the corrective action and the implementation of the corrective action. Remember: the cause analysis should correspond to the corrective action, and the evidence should correspond to the description of the corrective action and the corrective action.