C
Hi, I am seeking certification for a class IIa device for a very small manufacturer. I have a Post Market Surveillance Procedure in my QMS, but one of my non-conformances was that I need to include " a report on the surveillance or a justification as to why no surveillance was performed or documented".
We do normal monitoring of customer feedback and things like that but there have been no complaints or real problems to report.
How do I go about writing this report? Or does anyone know how to write a justification for not doing one? Any examples or advice helps!!!
Thanks so much
We do normal monitoring of customer feedback and things like that but there have been no complaints or real problems to report.
How do I go about writing this report? Or does anyone know how to write a justification for not doing one? Any examples or advice helps!!!
Thanks so much