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FDA Inspection 805111 — Vitalant

Vitalant — FEI 2970045

The FDA completed an inspection of Vitalant on October 19, 2012 in Fairfield, 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
October 19, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fairfield, CA (United States)

Facility

Other inspections at this facility

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  • 1059979 (NAI Mon Jul 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 975889 (NAI Wed Jun 29 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 893478 (NAI Wed Aug 27 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 728549 (NAI Wed Jun 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources