# FDA 483 - Dexcom, Inc. - June 14, 2024

Source: https://www.keypedia.com/records/483/dexcom-inc/824f979d-c9ac-43cf-b495-716a7fe418b5

> FDA 483 for Dexcom, Inc. on June 14, 2024. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Dexcom, Inc.
- Inspection Date: 2024-06-14
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - West V
- Summary: Dexcom, Inc. in Mesa, AZ, was inspected regarding its G6 and G7 Continuous Glucose Monitoring (CGM) sensors. The inspection revealed significant issues with inadequate documentation of process validation activities for sensor dipping formulations, including overly wide parameter ranges and insufficient verification of critical quality attributes. Additionally, the firm's corrective and preventive action procedures were found to be inadequately established, with several CAPA activities implemented prior to the CAPA creation or scope expansion.

## Related Officers

- [Deanna Bousalis](https://www.keypedia.com/people/deanna-bousalis/3737c5a1-8809-43a2-82f7-3e5154b2c4d4)
- [investigator](https://www.keypedia.com/people/maida-henesian/cd28e878-000c-4af8-8dbd-4863057758bb)

Company: https://www.keypedia.com/companies/dexcom-inc/951d0c4e-48b6-4963-9475-c905cf7fbf75

Office: https://www.keypedia.com/offices/division-of-human-and-animal-food-operations-west-v/0f4dd01e-8e8a-4336-9abe-ce8b3d309e8b