FDA Inspection 935795 — allphamed PHARBIL Arzneimittel GmbH

allphamed PHARBIL Arzneimittel GmbH — FEI 3008587095

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