FDA Warning Letter — Genus Medical Technologies
The FDA took a Warning Letter action against Genus Medical Technologies on May 2, 2017 (Chesterfield, MO). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.
Action Details
- Facility
- Genus Medical Technologies
- Date
- May 2, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Center
- CDER
- Location
- Chesterfield, MO (United States)