FDA Inspection 890864 — Vitalant

Vitalant — FEI 3007237324

The FDA completed an inspection of Vitalant on July 28, 2014 in Sparks, 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
July 28, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sparks, NV (United States)