FDA Inspection 1304042 — Octapharma plasma Inc.

Octapharma plasma Inc. — FEI 1073111

The FDA completed an inspection of Octapharma plasma Inc. on January 21, 2026 in Columbia, SC. 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
January 21, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Columbia, SC (United States)