FDA Inspection 906758 — Fresenius Kabi Austria Gmbh

Fresenius Kabi Austria Gmbh — FEI 3002807014

The FDA completed an inspection of Fresenius Kabi Austria Gmbh on Nov 7, 2014 in Linz. 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
Nov 7, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linz (Austria)

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