FDA Inspection 829223 — Vitalant

Vitalant — FEI 1771452

The FDA completed an inspection of Vitalant on Apr 22, 2013 in Fargo, ND. 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
Apr 22, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fargo, ND (United States)

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