FDA Inspection 1025477 — G. Pohl-Boskamp GmbH & Co. KG

G. Pohl-Boskamp GmbH & Co. KG — FEI 3002807915

The FDA completed an inspection of G. Pohl-Boskamp GmbH & Co. KG on September 15, 2017 in Hohenlockstedt. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 15, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hohenlockstedt (Germany)

Citations

IDCFRDescription
188321 CFR 211.165(a)Testing and release for distribution
202721 CFR 211.192Investigations of discrepancies, failures