Check the following points: - Each non-conformity is recorded and communicated to the levels where it was generated and/or detected- All non-conform product is identified (designation, quality status 'rejected' ) and isolated- Specific boxes or quarantine areas for ''rejected'' parts are available, with controlled access and without risk of mixing with other parts- Customers are informed promptly in the event that a nonconforming product has been shipped- Scraps are isolated in quarantine area with controlled access, until final elimination- Sorting, rework are performed in an isolated area under Written instructions- Nature of non-conformities, actions taken and deviations are registered and maintained=> 7 items fulfilled to validate procedure content