FDA Inspection 1171804 — Vitalant

Vitalant — FEI 1000114926

The FDA completed an inspection of Vitalant on June 6, 2022 in Lake Bluff, IL. 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 6, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lake Bluff, IL (United States)