FDA Inspection 1279648 — Allurion Technologies, Inc.

Allurion Technologies, Inc. — FEI 3011299930

The FDA completed an inspection of Allurion Technologies, Inc. on Aug 14, 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
Aug 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Natick, MA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.