# Becton Dickinson & Co. – FDA Inspection, Aug 4, 2017

Source: https://www.keypedia.com/records/fda_inspections/becton-dickinson-co/4087cbda-19d0-458b-bc67-d7fa565cd6b1
Source feed: FDA_Inspections

> FDA inspection 1020632 of Becton Dickinson & Co., August 04, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020632
- Company Name: Becton Dickinson & Co.
- Inspection Date: 2017-08-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Baltimore District Office
- Citation Count: 2

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- [FDA Inspection 1264435 - 2025-04-11](https://www.keypedia.com/records/fda_inspections/becton-dickinson-co/5024e704-6d78-4e5f-82ad-78bbb12a5b0f)
- FDA Inspection 1147022 - 2021-07-23
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- FDA Inspection 926020 - 2015-05-11

## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-m-simpson/3c0113ae-d846-4e37-aafa-13d58c465fa3)

Company: https://www.keypedia.com/companies/becton-dickinson-co/bbd4a72e-1db2-42b3-9c50-1c857692c743

Office: https://www.keypedia.com/offices/baltimore-district-office/6be371ff-03e9-4039-999c-ff170f17a9fa