FDA Inspection 1279648 — Allurion Technologies, Inc.

Allurion Technologies, Inc. — FEI 3011299930

The FDA completed an inspection of Allurion Technologies, Inc. on August 14, 2025 in Natick, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Natick, MA (United States)