# FDA Inspection 983232 - Allurion Technologies, Inc. - September 08, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/allurion-technologies-inc/48240f77-65e8-441b-b75b-5b3326c9a7e5
Source feed: FDA_Inspections

> FDA Inspection 983232 for Allurion Technologies, Inc. on September 08, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983232
- Company Name: Allurion Technologies, Inc.
- Inspection Date: 2016-09-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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