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FDA Inspection 676148 — Vitalant

Vitalant — FEI 1076019

The FDA completed an inspection of Vitalant on August 13, 2010 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
August 13, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Memphis, TN (United States)

Facility

Other inspections at this facility

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  • 1088977 (VAI Thu May 09 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1020983 (NAI Thu Jul 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 939332 (NAI Thu Aug 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources