FDA Inspection 1259448 — Vitalant

Vitalant — FEI 1523639

The FDA completed an inspection of Vitalant on January 24, 2025 in Elyria, OH. 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
January 24, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Elyria, OH (United States)