FDA Inspection 1227527 — Vitalant

Vitalant — FEI 1000124894

The FDA completed an inspection of Vitalant on December 21, 2023 in Glendale, AZ. 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
December 21, 2023
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Glendale, AZ (United States)