FDA Inspection 1264787 — Vitalant

Vitalant — FEI 1770181

The FDA completed an inspection of Vitalant on February 27, 2025 in Butte, MT. 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
February 27, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Butte, MT (United States)