FDA Inspection 1287158 — Allurion Technologies, Inc.

Allurion Technologies, Inc. — FEI 3011299930

The FDA completed an inspection of Allurion Technologies, Inc. on Oct 7, 2025 in Natick, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 7, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Natick, MA (United States)

Additional Details

Sponsor, Contract Research Organization

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