FDA Warning Letter — Generic Medical Devices, Inc.
The FDA took a Warning Letter action against Generic Medical Devices, Inc. on August 15, 2012 (Gig Harbor, WA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.
Action Details
- Facility
- Generic Medical Devices, Inc.
- Date
- August 15, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Center
- CDRH
- Location
- Gig Harbor, WA (United States)