FDA Inspection 611006 — Fresenius Kabi Austria GMBH

Fresenius Kabi Austria GMBH — FEI 3003708554

The FDA completed an inspection of Fresenius Kabi Austria GMBH on Jul 3, 2009 in Graz. 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 3, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Graz (Austria)

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