B
Bob the QE
We are prepping for our AS registration audit and we are struggling with an issue concerning audit cycles. We call in our ISO system that our QMS will be fully audited at a minimum of twice yearly, and we have met this. While prepping for our AS audit we are also keeping the ISO ball in the air. So our internal audit schedule was set to ISO. We did keep the twice a year requirement in the AS procedure, being we have not went through a complete year buy our AS audit I would not expect this to be a problem. Othere audits or assesments to AS9100 we have had in this year time frame are;
a) A GAP analysis - Findings detailed but not in CA form
b) We had one internal audit of the entire QMS to AS9100, CA's written.
c) One ISO audit of the entire QMS CA's written
d) An audit to AS9100 by a consultant. No formal CA's written.
e) Stage 1 and doc. review by our regristrar. CA's written.
Looking for opinions as to whether or not we may have a major issue just on the frequency or issua as to whether or not we have went through and entire audit cycle to AS9100?:mg:
a) A GAP analysis - Findings detailed but not in CA form
b) We had one internal audit of the entire QMS to AS9100, CA's written.
c) One ISO audit of the entire QMS CA's written
d) An audit to AS9100 by a consultant. No formal CA's written.
e) Stage 1 and doc. review by our regristrar. CA's written.
Looking for opinions as to whether or not we may have a major issue just on the frequency or issua as to whether or not we have went through and entire audit cycle to AS9100?:mg: