FDA Inspection 546260 — Pharbil Waltrop Gmbh

Pharbil Waltrop Gmbh — FEI 3004620586

The FDA completed an inspection of Pharbil Waltrop Gmbh on October 30, 2008 in Waltrop. 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
October 30, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Waltrop (Germany)