FDA Inspection
Becton, Dickinson and CompanyBecton, Dickinson and Company – FDA Inspection, May 18, 2017
Record Details
This FDA Inspection record concerns Becton, Dickinson and Company, with an inspection on May 18, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f41cf2be-bb3b-4860-9ebf-e26f88e447c5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1021270
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Becton, Dickinson and Company
5| Date | Classification | Office | Project area |
|---|---|---|---|
| March 23, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 20, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 13, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 30, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 24, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Becton, Dickinson and Company
- FDA Inspection 1201326 - 2023-03-23
- FDA Inspection 953011 - 2015-10-20
- FDA Inspection 919749 - 2015-03-13
- FDA Inspection 809304 - 2012-11-30
- FDA Inspection 578656 - 2009-04-24
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