FDA Inspection 571738 — Octapharma Plasma, Inc.
The FDA completed an inspection of Octapharma Plasma, Inc. on Mar 23, 2009 in Midfield, AL. 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 23, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Midfield, AL (United States)