# Allurion Technologies, Inc. - Inspection Records

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

> Inspection records and compliance data for Allurion Technologies, Inc. in Natick, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: Allurion Technologies, Inc.
- FEI Number: 3011299930
- City: Natick
- State: Massachusetts
- Country Name: United States
- Address Line 1: 14 Huron Dr
- Zip Code: 01760

## Related Documents

- [FDA Inspection 1287158 - Allurion Technologies, Inc. - 2025-10-07](https://www.globalkeysolutions.net/records/fda_inspections/allurion-technologies-inc/26818010-fb79-4524-9822-dfc243a607b2) — source: FDA, date: October 7, 2025
- [FDA Inspection 1287158 - Allurion Technologies, Inc. - 2025-10-07](https://www.globalkeysolutions.net/records/fda_inspections/allurion-technologies-inc/aeb81bb5-da7b-458d-8b3e-ad6c5f939b05) — classification: No Action Indicated (NAI), source: FDA, date: October 7, 2025
- [FDA Inspection 1279648 - Allurion Technologies, Inc. - 2025-08-14](https://www.globalkeysolutions.net/records/fda_inspections/allurion-technologies-inc/539ba891-96e8-42aa-9122-62577ae33f3f) — source: FDA, date: August 14, 2025
- [FDA Inspection 1279648 - Allurion Technologies, Inc. - 2025-08-14](https://www.globalkeysolutions.net/records/fda_inspections/allurion-technologies-inc/97d93a7b-aa4d-4399-b50a-5cd14c1fc468) — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2025
- [FDA Inspection 1279648 - Allurion Technologies, Inc. - 2025-08-14](https://www.globalkeysolutions.net/records/fda_inspections/allurion-technologies-inc/deb170c5-0cc1-4369-aa3f-54307a50616a) — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2025
- [FDA Inspection 983232 - Allurion Technologies, Inc. - 2016-09-08](https://www.globalkeysolutions.net/records/fda_inspections/allurion-technologies-inc/48240f77-65e8-441b-b75b-5b3326c9a7e5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 8, 2016

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