FDA Inspection 663451 — Cynosure, Inc.

Cynosure, Inc. — FEI 2428235

The FDA completed an inspection of Cynosure, Inc. on May 26, 2010 in Hicksville, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 26, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Hicksville, NY (United States)

Citations

IDCFRDescription
341621 CFR 820.70(a)(1)Process control instructions
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures