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FDA Inspection 608945 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3006604254

The FDA completed an inspection of Octapharma Plasma Inc on August 28, 2009 in Omaha, NE. 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
August 28, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Omaha, NE (United States)

Facility

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  • 909240 (VAI Thu Jan 08 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 820739 (NAI Wed Feb 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources