FDA Inspection 1085354 — Fresenius Kabi USA, LLC

Fresenius Kabi USA, LLC — FEI 1000115163

The FDA completed an inspection of Fresenius Kabi USA, LLC on Mar 8, 2019 in Melrose Park, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 8, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Melrose Park, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.