FDA Inspection 1206906 — Patheon Biologics B.V.

Patheon Biologics B.V. — FEI 3002608687

The FDA completed an inspection of Patheon Biologics B.V. on November 9, 2021 in Groningen. 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 9, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Groningen (Netherlands)

Additional Details

Mutual Recognition Agreement (MRA)