FDA Inspection 897983 — Fresenius Kabi USA, LLC

Fresenius Kabi USA, LLC — FEI 3002733956

The FDA completed an inspection of Fresenius Kabi USA, LLC on October 6, 2014 in Lake Zurich, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 6, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lake Zurich, IL (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)