FDA Inspection 635692 — Vitalant

Vitalant — FEI 1000139692

The FDA completed an inspection of Vitalant on December 22, 2009 in Rio Rancho, 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
December 22, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rio Rancho, NM (United States)