FDA Inspection 741633 — Fresenius Kabi Austria Gmbh

Fresenius Kabi Austria Gmbh — FEI 3002807014

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

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