# Allurion Technologies, Inc. – FDA Inspection, Sep 8, 2016

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

> FDA inspection 983232 of Allurion Technologies, Inc., September 08, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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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