FDA Inspection 792432 — Vitalant

Vitalant — FEI 3002643000

The FDA completed an inspection of Vitalant on Jul 19, 2012 in Scottsdale, AZ. 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
Jul 19, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Scottsdale, AZ (United States)