Home / Inspections / 816229

FDA Inspection 816229 — 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 18, 2012 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 18, 2012
Fiscal Year
2013
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))
  • 918160 (VAI Thu Mar 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources