FDA Inspection 729457 — Vitalant

Vitalant — FEI 3000717794

The FDA completed an inspection of Vitalant on June 9, 2011 in Las Vegas, NV. 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
June 9, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Vegas, NV (United States)