FDA Inspection 766939 — Octapharma Plasma, Inc.
The FDA completed an inspection of Octapharma Plasma, Inc. on February 3, 2012 in Virginia Beach, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- February 3, 2012
- Fiscal Year
- 2012
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Virginia Beach, VA (United States)