FDA Inspection 884687 — Vitalant

Vitalant — FEI 1000123788

The FDA completed an inspection of Vitalant on June 25, 2014 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
June 25, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Carson City, NV (United States)