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FDA Inspection 779864 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007166613

The FDA completed an inspection of Octapharma Plasma, Inc. on April 5, 2012 in Newport News, 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
April 5, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Newport News, VA (United States)

Facility

Other inspections at this facility

  • 1132304 (NAI Wed Oct 14 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1069326 (NAI Wed Sep 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 970304 (VAI Fri Apr 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865923 (NAI Tue Feb 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources