FDA Inspection 1125102 — BIPSO GmbH

BIPSO GmbH — FEI 3009099058

The FDA completed an inspection of BIPSO GmbH on November 7, 2019 in Singen (Hohentwiel). 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
November 7, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Singen (Hohentwiel) (Germany)

Additional Details

Mutual Recognition Agreement (MRA)