FDA Inspection 1320244 — Vitalant

Vitalant — FEI 3003370237

The FDA completed an inspection of Vitalant on May 29, 2026 in Chicago, IL. 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
May 29, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chicago, IL (United States)