FDA Inspection 1251496 — Vitalant

Vitalant — FEI 1671462

The FDA completed an inspection of Vitalant on August 2, 2024 in Albuquerque, NM. 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
August 2, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Albuquerque, NM (United States)