FDA Inspection 701076 — Vitalant

Vitalant — FEI 1000522999

The FDA completed an inspection of Vitalant on Dec 6, 2010 in Davis, CA. 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
Dec 6, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Davis, CA (United States)

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