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FDA Inspection 935859 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007507466

The FDA completed an inspection of Octapharma Plasma, Inc. on July 23, 2015 in Des Moines, 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
July 23, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Des Moines, IA (United States)

Facility

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  • 1015098 (NAI Tue May 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 819769 (NAI Thu Feb 21 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 722288 (NAI Mon May 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 660401 (VAI Thu May 06 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources