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FDA Inspection 1153683 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006468609

The FDA completed an inspection of Octapharma Plasma, Inc. on September 23, 2021 in Wichita, KS. 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
September 23, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wichita, KS (United States)

Facility

Other inspections at this facility

  • 1322600 (NAI Fri May 15 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1008990 (NAI Thu Mar 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 916482 (NAI Thu Mar 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 757171 (NAI Thu Dec 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 649786 (NAI Wed Mar 03 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources