FDA Warning Letter — TriMed Inc.
The FDA took a Warning Letter action against TriMed Inc. on June 30, 2016 (Valencia, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- TriMed Inc.
- Date
- June 30, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Center
- CDRH
- Location
- Valencia, CA (United States)