FDA Inspection 608986 — Vitalant

Vitalant — FEI 1000139516

The FDA completed an inspection of Vitalant on August 25, 2009 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
August 25, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Cruces, NM (United States)