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FDA Inspection 923869 — Vitalant

Vitalant — FEI 1671462

The FDA completed an inspection of Vitalant on April 15, 2015 in Albuquerque, NM. 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
April 15, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Albuquerque, NM (United States)

Facility

Other inspections at this facility

  • 1251496 (NAI Fri Aug 02 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1118232 (NAI Fri Jan 10 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1044582 (NAI Fri Dec 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 980906 (NAI Thu Jun 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 808877 (VAI Fri Nov 30 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources