Checkout MedtechInsight'sUSFDAWarningLetterDataTracker here.
This chart lists device-related warning letters released by the US Food and Drug Administration in December 2021
Quality systems and Medical Device Reporting violations were noted by US FDA investigators during an on-site inspection of Medtronic’s Northridge, CA, facility. A total of seven device-related warning letters were released by the agency last month.
Checkout MedtechInsight'sUSFDAWarningLetterDataTracker here.
This chart lists device-related warning letters released by the US Food and Drug Administration in December 2021