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FDA Inspection 1021270 — Becton, Dickinson and Company

Becton, Dickinson and Company — FEI 1917413

The FDA completed an inspection of Becton, Dickinson and Company on May 18, 2017 in Broken Bow, 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
May 18, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Broken Bow, NE (United States)

Facility

Other inspections at this facility

  • 1201326 (NAI Thu Mar 23 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 953011 (NAI Tue Oct 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919749 (NAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809304 (NAI Fri Nov 30 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 578656 (NAI Fri Apr 24 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources