FDA Inspection 1209112 — Vitalant

Vitalant — FEI 2377742

The FDA completed an inspection of Vitalant on June 21, 2023 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
June 21, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Baton Rouge, LA (United States)