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FDA Inspection 789482 — Vitalant

Vitalant — FEI 3007101464

The FDA completed an inspection of Vitalant on June 22, 2012 in Mather, CA. 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 22, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mather, CA (United States)

Facility

Other inspections at this facility

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  • 1098166 (NAI Thu Jul 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984109 (NAI Thu Aug 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 895712 (VAI Fri Sep 12 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 604009 (VAI Tue Aug 04 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources