FDA Inspection 1338152 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3015616951

The FDA completed an inspection of Octapharma Plasma Inc on Sep 3, 2026 in Birmingham, AL. 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 3, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Birmingham, AL (United States)