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FDA Inspection 542074 — Vitalant

Vitalant — FEI 2371456

The FDA completed an inspection of Vitalant on October 20, 2008 in Lafayette, LA. 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 20, 2008
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lafayette, LA (United States)

Facility

Other inspections at this facility

  • 1231512 (NAI Thu Jul 11 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094101 (VAI Wed Jun 19 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 993571 (NAI Tue Oct 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984244 (NAI Thu Aug 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 879849 (NAI Fri May 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources