P
ppalm
Hi
I am confused.
It´s clear for me that you must do som kind of MSA on the evaluations teqnices specified in the controlplan.
Say that there is an item in the controlplan for "processing foil" that says that you measure the gloss 1:sample/each batch. In this case its verry clear for me that the "gloss meassuring" shall have some kind of MSA studie done.
But say that there is going to be an uppdate the foil for, example new grain/pattern. This new "status" is testet/validated according to an validation plan in an internal laboratory and the internal laboratory measured the grain.
Shall the internal laboratory make MSA studies for such items?
On wich item can i as an intarnal ISO/TS auditor make nonconformity note?
Best regards Patrik
I am confused.
It´s clear for me that you must do som kind of MSA on the evaluations teqnices specified in the controlplan.
Say that there is an item in the controlplan for "processing foil" that says that you measure the gloss 1:sample/each batch. In this case its verry clear for me that the "gloss meassuring" shall have some kind of MSA studie done.
But say that there is going to be an uppdate the foil for, example new grain/pattern. This new "status" is testet/validated according to an validation plan in an internal laboratory and the internal laboratory measured the grain.
Shall the internal laboratory make MSA studies for such items?
On wich item can i as an intarnal ISO/TS auditor make nonconformity note?
Best regards Patrik