FDA Inspection 722395 — Vitalant

Vitalant — FEI 3003603165

The FDA completed an inspection of Vitalant on Apr 28, 2011 in Naperville, IL. 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
Apr 28, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Naperville, IL (United States)