FDA Inspection 1297232 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3014123102

The FDA completed an inspection of Octapharma Plasma Inc on December 11, 2025 in Santa Fe Springs, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 11, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Fe Springs, CA (United States)

Citations

IDCFRDescription
8021 CFR 606.100(b)(1)Donor criteria