FDA Inspection 1211673 — Vitalant

Vitalant — FEI 3003751010

The FDA completed an inspection of Vitalant on August 2, 2023 in Lewiston, ID. 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, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lewiston, ID (United States)