FDA Inspection 902077 — Vitalant

Vitalant — FEI 3002961879

The FDA completed an inspection of Vitalant on October 30, 2014 in Gurnee, 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 30, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Gurnee, IL (United States)