FDA Inspection 1256136 — Vitalant

Vitalant — FEI 3013133006

The FDA completed an inspection of Vitalant on November 14, 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 14, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Spokane, WA (United States)