FDA Inspection 1207391 — Fresenius Kabi Austria GMBH

Fresenius Kabi Austria GMBH — FEI 3003708554

The FDA completed an inspection of Fresenius Kabi Austria GMBH on October 13, 2022 in Graz. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 13, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Graz (Austria)

Additional Details

Mutual Recognition Agreement (MRA)