# Dexcom, Inc. – FDA Inspection, Feb 16, 2018

Source: https://www.keypedia.com/records/fda_inspections/dexcom-inc/e2472c3d-9870-4181-b652-d7105450f55b
Source feed: FDA_Inspections

> FDA inspection 1041434 of Dexcom, Inc., February 16, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1041434
- Company Name: Dexcom, Inc.
- Inspection Date: 2018-02-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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- FDA Inspection 1220386 - 2023-09-29
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- [FDA Inspection 965585 - 2016-03-29](https://www.keypedia.com/records/fda_inspections/dexcom-inc/7fb828e6-b61a-4d4b-85e5-12fcf3a495c7)
- FDA Inspection 923017 - 2015-04-21

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/andrea-a-branche/9ffe9b53-7963-49a6-be4e-25e644f1759f)

Company: https://www.keypedia.com/companies/dexcom-inc/e6b9b288-fede-4673-88ef-fd37fc036366

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