FDA Inspection 1266226 — Vitalant

Vitalant — FEI 2377742

The FDA completed an inspection of Vitalant on April 2, 2025 in Baton Rouge, LA. 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
April 2, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Baton Rouge, LA (United States)