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FDA Inspection 1200172 — Patheon Biologics LLC

Patheon Biologics LLC — FEI 3003418999

The FDA completed an inspection of Patheon Biologics LLC on March 2, 2023 in Saint Louis, MO. 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
March 2, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)

Facility

Other inspections at this facility

  • 1251864 (VAI Wed Nov 20 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1224734 (VAI Fri Dec 08 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1099387 (VAI Fri Aug 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867704 (VAI Fri Feb 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 775547 (NAI Tue Apr 03 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources