# Becton, Dickinson and Company – FDA Inspection, May 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/becton-dickinson-and-company/f41cf2be-bb3b-4860-9ebf-e26f88e447c5
Source feed: FDA_Inspections

> FDA inspection 1021270 of Becton, Dickinson and Company, May 18, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021270
- Company Name: Becton, Dickinson and Company
- Inspection Date: 2017-05-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- 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

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)
- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

Company: https://www.keypedia.com/companies/becton-dickinson-and-company/4e5ec8a1-50ec-4768-a829-49509a3affe0

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7