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FDA Inspection 838033 — Octapharma Plasma, Inc. Portsmouth

Octapharma Plasma, Inc. Portsmouth — FEI 3007166600

The FDA completed an inspection of Octapharma Plasma, Inc. Portsmouth on June 20, 2013 in Portsmouth, 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
June 20, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portsmouth, VA (United States)

Facility

Other inspections at this facility

  • 1137609 (NAI Tue Mar 30 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066750 (VAI Wed Sep 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 992370 (VAI Fri Oct 28 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 733852 (VAI Tue Jun 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources