FDA Inspection 1258010 — Vitalant

Vitalant — FEI 3071345

The FDA completed an inspection of Vitalant on November 22, 2024 in Spokane, WA. 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 22, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Spokane, WA (United States)