FDA Inspection 898141 — Octapharma Plasma, Inc.
The FDA completed an inspection of Octapharma Plasma, Inc. on September 11, 2014 in Virginia Beach, 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
- September 11, 2014
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Virginia Beach, VA (United States)