FDA Inspection 1109758 — Vitalant

Vitalant — FEI 1000515229

The FDA completed an inspection of Vitalant on October 24, 2019 in Lansing, 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
October 24, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lansing, IL (United States)