FDA Inspection 663210 — Vitalant

Vitalant — FEI 1000123788

The FDA completed an inspection of Vitalant on May 24, 2010 in Carson City, 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
May 24, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Carson City, NV (United States)