FDA Inspection 905902 — Vitalant

Vitalant — FEI 3002614029

The FDA completed an inspection of Vitalant on December 5, 2014 in El Paso, TX. 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
December 5, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
El Paso, TX (United States)