FDA Inspection 907184 — Vitalant

Vitalant — FEI 3003370237

The FDA completed an inspection of Vitalant on December 16, 2014 in Chicago, 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
December 16, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chicago, IL (United States)