FDA Inspection 1256346 — Vitalant

Vitalant — FEI 3001831403

The FDA completed an inspection of Vitalant on November 13, 2024 in Coeur D Alene, ID. 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
November 13, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Coeur D Alene, ID (United States)