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FDA Inspection 806330 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3005621840

The FDA completed an inspection of Octapharma Plasma, Inc. on October 25, 2012 in Monroe, LA. 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
October 25, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Monroe, LA (United States)

Facility

Other inspections at this facility

  • 1089657 (NAI Wed Apr 24 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 976436 (NAI Thu Jun 30 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 614657 (NAI Thu Sep 24 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources