FDA Inspection 920722 — Vitalant
The FDA completed an inspection of Vitalant on April 2, 2015 in Hattiesburg, 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
- April 2, 2015
- Fiscal Year
- 2015
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Hattiesburg, MS (United States)