FDA Inspection 798540 — Vitalant

Vitalant — FEI 1000221376

The FDA completed an inspection of Vitalant on September 12, 2012 in Henderson, 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
September 12, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Henderson, NV (United States)