FDA Inspection 1295718 — Vitalant

Vitalant — FEI 3012336081

The FDA completed an inspection of Vitalant on December 10, 2025 in Parker, CO. 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 10, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Parker, CO (United States)