FDA Inspection 1199272 — Fresenius Kabi Austria Gmbh

Fresenius Kabi Austria Gmbh — FEI 3002807014

The FDA completed an inspection of Fresenius Kabi Austria Gmbh on Jul 15, 2021 in Linz. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 15, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linz (Austria)

Additional Details

Mutual Recognition Agreement (MRA)

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