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FDA Inspection 783512 — Vitalant

Vitalant — FEI 1076019

The FDA completed an inspection of Vitalant on April 27, 2012 in Memphis, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 27, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Memphis, TN (United States)

Facility

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FDA data resources