FDA Inspection 1231512 — Vitalant

Vitalant — FEI 2371456

The FDA completed an inspection of Vitalant on July 11, 2024 in Lafayette, 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
July 11, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lafayette, LA (United States)