FDA Inspection 741633 — Fresenius Kabi Austria Gmbh

Fresenius Kabi Austria Gmbh — FEI 3002807014

The FDA completed an inspection of Fresenius Kabi Austria Gmbh on July 29, 2011 in Linz. 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
July 29, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linz (Austria)