Medical device production is completed why should be cleaned and recorded

A: In accordance with the provisions of the Code for Quality Management of Medical Device Manufacturing (for trial implementation), must be produced in accordance with the requirements of the Code, as follows:

Article 32 In the production process must be cleaned to deal with or to remove from the product to deal with the material, the production enterprise shall be cleaned to the product of the requirements of the formation of the document and its implementation. Contamination of sterile medical devices should be controlled and the sterilization process.

Article 33 If the results of the production process can not or can not be easily verified by subsequent inspection and testing, the process shall be confirmed. Records of confirmation activities and results shall be maintained. The producer shall qualify the process validation personnel.

So, after the completion of the production of medical devices should be cleared and recorded to prevent errors and ensure the production of qualified products.