The question has been raised what if a part is not made to drawing. This will give a potential failure. Surely this is not the responsibilty of the designer how far do I need to go with this. Even if we look at every dimension on the drawing we still can not stop the part being manufactured...
So can I be clear on this. Once you have calculated the risk and have tests on prototypes to back up your design calculations, Then leaving the recommended actions is ok
I am currently conducting an fmea on a system and am a bit confused on the design verification column. If there are calculations and existing test procedures that have been carried out at the design stage. Does this necessarily mean that you have to fill in the recommended action columns?
