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FDA Inspection 1194258 — Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.

Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. — FEI 3002809097

The FDA completed an inspection of Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. on December 16, 2022 in Vienna. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 16, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Vienna (Austria)

Facility

Other inspections at this facility

  • 1090370 (VAI Tue Apr 16 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1002598 (VAI Tue Jan 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 918160 (VAI Thu Mar 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 816229 (VAI Tue Dec 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources