FDA Inspection 742569 — Miltenyi Biotec Gmbh

Miltenyi Biotec Gmbh — FEI 3004112148

The FDA completed an inspection of Miltenyi Biotec Gmbh on Aug 18, 2011 in Bergisch Gladbach. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 18, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bergisch Gladbach (Germany)

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