FDA Inspection 906138 — Vitalant

Vitalant — FEI 1000139516

The FDA completed an inspection of Vitalant on November 20, 2014 in Las Cruces, NM. 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
November 20, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Cruces, NM (United States)