FDA Inspection 1292886 — Vitalant

Vitalant — FEI 1471533

The FDA completed an inspection of Vitalant on November 19, 2025 in Schaumburg, 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
November 19, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Schaumburg, IL (United States)