Cenova welcomes the FDA for a routine inspection – another excellent outcome

During the month of May, Cenova once again welcomed FDA for a routine QSIT inspection, the third time in the last decade. The background is Cenovas extensive and wide scope of listed PMAs and 510(k)s where Cenova is the full scope contract manufacturer.

The inspection lasted for several days and once again resulted in an excellent outcome. As always, inspections and audits not only confirm how good we are, but it also results in room for improvement, and we love it. It keeps us best in class and up to date with global best practices.

We truly appreciate the opportunity to host the FDA, as well as our customers Notified Bodies. And of course – yes, we’re proud of the result.