FDA Inspection 1236502 — Vitalant

Vitalant — FEI 3002572707

The FDA completed an inspection of Vitalant on Apr 4, 2024 in Oak Lawn, IL. 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
Apr 4, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Oak Lawn, IL (United States)