FDA Inspection 1300064 — Octapharma Plasma Inc
The FDA completed an inspection of Octapharma Plasma Inc on January 16, 2026 in Kansas City, 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
- January 16, 2026
- Fiscal Year
- 2026
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Kansas City, KS (United States)