FDA Inspection 712769 — Vitalant

Vitalant — FEI 1000139516

The FDA completed an inspection of Vitalant on February 22, 2011 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
February 22, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Cruces, NM (United States)