FDA Inspection 1305000 — Vitalant

Vitalant — FEI 3000717965

The FDA completed an inspection of Vitalant on February 12, 2026 in Canton, 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
February 12, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Canton, OH (United States)