FDA Warning Letter — Turbare Manufacturing
The FDA took a Warning Letter action against Turbare Manufacturing on September 16, 2025 (Conway, AR). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- Turbare Manufacturing
- Date
- September 16, 2025
- Fiscal Year
- 2025
- Product Type
- Drugs
- Center
- CDER
- Location
- Conway, AR (United States)