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FDA Inspection 1214415 — BD Medical

BD Medical — FEI 1920898

The FDA completed an inspection of BD Medical on August 2, 2023 in Holdrege, NE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 2, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Holdrege, NE (United States)

Facility

Other inspections at this facility

  • 1229942 (NAI Thu Sep 12 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1034313 (NAI Wed Nov 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 985211 (NAI Thu Jul 28 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 942641 (VAI Thu Aug 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 918912 (NAI Thu Mar 19 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources