FDA Inspection 1137609 — Octapharma Plasma, Inc. Portsmouth
The FDA completed an inspection of Octapharma Plasma, Inc. Portsmouth on Mar 30, 2021 in Portsmouth, VA. 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
- Mar 30, 2021
- Fiscal Year
- 2021
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Portsmouth, VA (United States)