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FDA Inspection 1017592 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 2077760

The FDA completed an inspection of Octapharma Plasma Inc on June 9, 2017 in Van Nuys, CA. 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 9, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Van Nuys, CA (United States)

Facility

Other inspections at this facility

  • 1252471 (NAI Thu Jan 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 937941 (NAI Wed Aug 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 827645 (VAI Fri Apr 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 685909 (VAI Thu Sep 30 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources