FDA Inspection 1281750 — Vitalant
The FDA completed an inspection of Vitalant on August 29, 2025 in Rapid City, SD. 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
- August 29, 2025
- Fiscal Year
- 2025
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Rapid City, SD (United States)