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FDA Inspection 767449 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 1035346

The FDA completed an inspection of Octapharma Plasma, Inc. on February 2, 2012 in Jacksonville, FL. 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
February 2, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Jacksonville, FL (United States)

Facility

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  • 902074 (NAI Wed Oct 29 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 792075 (NAI Thu Jul 26 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources