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FDA Inspection 918160 — 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 March 5, 2015 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
March 5, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Vienna (Austria)

Facility

Other inspections at this facility

  • 1194258 (VAI Fri Dec 16 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 816229 (VAI Tue Dec 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources