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FDA Inspection 759822 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3007743657

The FDA completed an inspection of Octapharma Plasma Inc on December 13, 2011 in Sioux City, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 13, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sioux City, IA (United States)

Facility

Other inspections at this facility

  • 1153080 (NAI Thu Sep 09 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1008992 (NAI Thu Mar 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 920586 (VAI Wed Apr 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 780527 (NAI Thu May 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources