Home / Inspections / 578656

FDA Inspection 578656 — Becton, Dickinson and Company

Becton, Dickinson and Company — FEI 1917413

The FDA completed an inspection of Becton, Dickinson and Company on April 24, 2009 in Broken Bow, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 24, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: 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))
  • 1021270 (VAI Thu May 18 2017 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))

FDA data resources