I
IBATE
Newbie here. I am responsible for developing/maintaining ATE's for a number of complex electronic modules for product validation testing - not manufacturing. Little or no operator variation.
1) Is a gage R&R appropriate or would the process better be described as a Capability Analysis? ANOVA OK for this?
2) I cannot produce samples that consistently fall into lower/upper limits of the spec. range(s) due to cost, etc. How do I get around this?
3) Anyone have a process defined for this situation?
4) FMEA recommended to insure all out of spec. values are captured?
Appreciate any comments - I can't be the only one wrestling with this one.
1) Is a gage R&R appropriate or would the process better be described as a Capability Analysis? ANOVA OK for this?
2) I cannot produce samples that consistently fall into lower/upper limits of the spec. range(s) due to cost, etc. How do I get around this?
3) Anyone have a process defined for this situation?
4) FMEA recommended to insure all out of spec. values are captured?
Appreciate any comments - I can't be the only one wrestling with this one.