FDA Inspection 550851 — Vitalant

Vitalant — FEI 3007237324

The FDA completed an inspection of Vitalant on December 5, 2008 in Sparks, NV. 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, 2008
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sparks, NV (United States)