FDA Inspection
Allurion Technologies, Inc.Allurion Technologies, Inc. – FDA Inspection, Sep 8, 2016
Record Details
This FDA Inspection record concerns Allurion Technologies, Inc., with an inspection on September 8, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Allurion Technologies, Inc.
- Inspection Date
- September 8, 2016
- Product Type
- Devices
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ID · 48240f77-65e8-441b-b75b-5b3326c9a7e5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 983232
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.30(d)Design output - documentation
- 21 CFR 820.75(a)Documentation
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Other FDA inspections of Allurion Technologies, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 7, 2025 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| August 14, 2025 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Allurion Technologies, Inc.
- FDA Inspection 1287158 - 2025-10-07
- FDA Inspection 1279648 - 2025-08-14
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