FDA Inspection
Becton Dickinson And CompanyBecton Dickinson And Company – FDA Inspection, May 12, 2017
Record Details
This FDA Inspection record concerns Becton Dickinson And Company, with an inspection on May 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a9dcc961-22b3-4b4f-96e5-c693d19ead95
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1012404
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Becton Dickinson And Company
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 11, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 11, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 21, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 27, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Becton Dickinson And Company
- FDA Inspection 985379 - 2016-08-11
- FDA Inspection 847638 - 2013-09-11
- FDA Inspection 723716 - 2011-04-21
- FDA Inspection 607365 - 2009-08-27
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