FDA Warning Letter — Fresenius Kabi USA, LLC

Case 225954 — FEI 3001833549

The FDA took a Warning Letter action against Fresenius Kabi USA, LLC on February 22, 2012 (Grand Island, NY). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Fresenius Kabi USA, LLC
Date
February 22, 2012
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Grand Island, NY (United States)