FDA Inspection 962804 — Vitalant

Vitalant — FEI 1000123788

The FDA completed an inspection of Vitalant on March 16, 2016 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
March 16, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Carson City, NV (United States)