FDA Inspection 745654 — Cynosure, LLC

Cynosure, LLC — FEI 1000120578

The FDA completed an inspection of Cynosure, LLC on Sep 15, 2011 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
Sep 15, 2011
Fiscal Year
2011
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.