FDA Warning Letter — Fresenius Kabi USA LLC (FK USA)
The FDA took a Warning Letter action against Fresenius Kabi USA LLC (FK USA) on Jan 28, 2011 (Bensenville, IL). 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 (FK USA)
- Date
- Jan 28, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Center
- CDRH
- Location
- Bensenville, IL (United States)