FDA Inspection 736493 — Vitalant

Vitalant — FEI 1771461

The FDA completed an inspection of Vitalant on Jul 27, 2011 in Billings, MT. 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
Jul 27, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Billings, MT (United States)

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