FDA Inspection 682645 — Vitalant
The FDA completed an inspection of Vitalant on Aug 30, 2010 in Tupelo, MS. 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
- Aug 30, 2010
- Fiscal Year
- 2010
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Tupelo, MS (United States)