FDA Inspection 962801 — Vitalant

Vitalant — FEI 3007237324

The FDA completed an inspection of Vitalant on Mar 15, 2016 in Sparks, 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
Mar 15, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sparks, NV (United States)

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