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FDA Inspection 985379 — Becton Dickinson And Company

Becton Dickinson And Company — FEI 1911916

The FDA completed an inspection of Becton Dickinson And Company on August 11, 2016 in Columbus, 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 11, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, NE (United States)

Facility

Other inspections at this facility

  • 1012404 (VAI Fri May 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847638 (NAI Wed Sep 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 723716 (VAI Thu Apr 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 607365 (VAI Thu Aug 27 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources