FDA Inspection 729747 — Vitalant
The FDA completed an inspection of Vitalant on June 7, 2011 in Southaven, MS. 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
- June 7, 2011
- Fiscal Year
- 2011
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Southaven, MS (United States)