FDA Inspection 1132304 — Octapharma Plasma, Inc.
The FDA completed an inspection of Octapharma Plasma, Inc. on October 14, 2020 in Newport News, VA. 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
- October 14, 2020
- Fiscal Year
- 2021
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Newport News, VA (United States)