FDA Inspection 968492 — Vitalant

Vitalant — FEI 3009953178

The FDA completed an inspection of Vitalant on Mar 11, 2016 in Colorado Springs, CO. 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
Mar 11, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Colorado Springs, CO (United States)