FDA Inspection 1003091 — Cynosure, LLC

Cynosure, LLC — FEI 1000120578

The FDA completed an inspection of Cynosure, LLC on Mar 13, 2017 in Westford, 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
Mar 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Westford, MA (United States)

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