FDA Inspection 1277492 — Vitalant

Vitalant — FEI 1771461

The FDA completed an inspection of Vitalant on July 18, 2025 in Billings, 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
July 18, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Billings, MT (United States)