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FDA Inspection 986835 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006402207

The FDA completed an inspection of Octapharma Plasma, Inc. on August 31, 2016 in Petersburg, VA. 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 31, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Petersburg, VA (United States)

Facility

Other inspections at this facility

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  • 1044209 (NAI Thu Feb 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865407 (NAI Fri Jan 31 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 767837 (VAI Tue Jan 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 664473 (NAI Wed May 26 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources