FDA Inspection 768754 — Cynosure, LLC

Cynosure, LLC — FEI 1000120578

The FDA completed an inspection of Cynosure, LLC on Feb 17, 2012 in Westford, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 17, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Westford, MA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures

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