FDA Inspection 952599 — Vitalant

Vitalant — FEI 3004573369

The FDA completed an inspection of Vitalant on Dec 17, 2015 in Orland Park, 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
Dec 17, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Orland Park, IL (United States)