FDA Inspection 865572 — Octapharma Plasma, Inc.
The FDA completed an inspection of Octapharma Plasma, Inc. on February 6, 2014 in Ypsilanti, MI. 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 6, 2014
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Ypsilanti, MI (United States)