FDA Inspection 1338640 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007587556

The FDA completed an inspection of Octapharma Plasma, Inc. on Sep 18, 2026 in Lubbock, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 18, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lubbock, TX (United States)