FDA Inspection 1329700 — Vitalant

Vitalant — FEI 3014028220

The FDA completed an inspection of Vitalant on Jul 23, 2026 in Spokane Valley, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 23, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Spokane Valley, WA (United States)