FDA Inspection 1058148 — Vitalant

Vitalant — FEI 3004626441

The FDA completed an inspection of Vitalant on May 25, 2018 in Flagstaff, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 25, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Flagstaff, AZ (United States)