# Allurion Technologies, Inc. – FDA Inspection, Aug 14, 2025

Source: https://www.keypedia.com/records/fda_inspections/allurion-technologies-inc/deb170c5-0cc1-4369-aa3f-54307a50616a
Source feed: FDA_Inspections

> FDA inspection 1279648 of Allurion Technologies, Inc., August 14, 2025. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279648
- Company Name: Allurion Technologies, Inc.
- Inspection Date: 2025-08-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- 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 1287158 - 2025-10-07
- [FDA Inspection 983232 - 2016-09-08](https://www.keypedia.com/records/fda_inspections/allurion-technologies-inc/48240f77-65e8-441b-b75b-5b3326c9a7e5)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/matthew-w-kyle/0f297104-ae6c-4fc4-a240-c84e5e907803)
- [Issuing Officer](https://www.keypedia.com/people/monica-l-gutierrez/fe60f8c6-ad1b-4619-9903-ed7be6d3bf7d)

Company: https://www.keypedia.com/companies/allurion-technologies-inc/e92baf10-66f9-4dae-a6a3-2b10e486ebdf

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