M
MrOctober
I'm going through some RCA from a recent AS9100 audit.
They are requiring that I submit "corrections."
I've submitted the corrective actions and the root causes and all were accepted. There were no high risk findings just small procedural changes that did not require any containment action and had no effect on end product and did not effect our customers. I ended up having to remove or reword some clauses from our QMS system that painted ourselves in a corner for being too specific. The clauses were too specific in that they were required by our QMS system but not practiced because it was non value added essentially. The clauses also made it almost impossible to comply because they were written when our company was a lot smaller and we've nearly tripled in size since then. So the changes were just procedural and documentation.
They are requiring that I submit "corrections."
I've submitted the corrective actions and the root causes and all were accepted. There were no high risk findings just small procedural changes that did not require any containment action and had no effect on end product and did not effect our customers. I ended up having to remove or reword some clauses from our QMS system that painted ourselves in a corner for being too specific. The clauses were too specific in that they were required by our QMS system but not practiced because it was non value added essentially. The clauses also made it almost impossible to comply because they were written when our company was a lot smaller and we've nearly tripled in size since then. So the changes were just procedural and documentation.