FDA Inspection 729457 — Vitalant

Vitalant — FEI 3000717794

The FDA completed an inspection of Vitalant on Jun 9, 2011 in Las Vegas, NV. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 9, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Vegas, NV (United States)

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