FDA Inspection 1223522 — Vitalant

Vitalant — FEI 2071464

The FDA completed an inspection of Vitalant on Nov 9, 2023 in Tempe, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 9, 2023
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tempe, AZ (United States)