In this week’s lecture, Dr. Simon discussed about nonconforming product and how action must be taken to make sure the DMR requirements are met. In addition, any rework must be completed before releasing the product into market.
Does anyone have any experience or examples of nonconforming product and personally seeing the flow into a CAPA? Also, what can be some reasons for the nonconforming product to occur in the first place and can the chance of occurring be reduced?