FDA Inspection 927824 — Vitalant

Vitalant — FEI 1000135466

The FDA completed an inspection of Vitalant on April 30, 2015 in Mesa, AZ. 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
April 30, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mesa, AZ (United States)