FDA Inspection 1310204 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3023193589

The FDA completed an inspection of Octapharma Plasma Inc on March 19, 2026 in Denver, CO. 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
March 19, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Denver, CO (United States)