FDA Inspection 1298618 — Octapharma Plasma, Inc.
The FDA completed an inspection of Octapharma Plasma, Inc. on Jan 9, 2026 in West Covina, CA. 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
- Jan 9, 2026
- Fiscal Year
- 2026
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- West Covina, CA (United States)