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FDA Inspection 1017789 — Vitalant

Vitalant — FEI 1000143480

The FDA completed an inspection of Vitalant on June 16, 2017 in Aberdeen, SD. 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
June 16, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aberdeen, SD (United States)

Facility

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