FDA Warning Letter — Fresenius Kabi USA, LLC
The FDA took a Warning Letter action against Fresenius Kabi USA, LLC on Jan 4, 2024 (North Andover, MA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.
Action Details
- Facility
- Fresenius Kabi USA, LLC
- Date
- Jan 4, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Center
- CDRH
- Location
- North Andover, MA (United States)