FDA Warning Letter — Biomet, Inc.
The FDA took a Warning Letter action against Biomet, Inc. on July 27, 2010 (Warsaw, IN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Biomet, Inc.
- Date
- July 27, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Warsaw, IN (United States)