FDA Inspection 935795 — Allphamed PHARBIL Arzneimittel GmbH

Allphamed PHARBIL Arzneimittel GmbH — FEI 3008587095

The FDA completed an inspection of Allphamed PHARBIL Arzneimittel GmbH on Jul 10, 2015 in Gottingen. 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 10, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gottingen (Germany)

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