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FDA Inspection
•Cynosure, Llc•December 14, 2018

Cynosure, Llc – FDA Inspection, Dec 14, 2018

Record Details

This FDA Inspection record concerns Cynosure, Llc, with an inspection on December 14, 2018, issued by the New England District Office, covering medical devices & rad health.

Company
Cynosure, Llc
Inspection Date
December 14, 2018
Product Type
Medical Devices & Rad Health
Office
New England District Office
View Company Profile

ID · 496233e7-a1ec-4920-8837-6599139560c0

Inspection Facts

Inspection number
1093281
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Cynosure, Llc

9
DateClassificationOfficeProject area
December 12, 2025NAICenter for Devices and Radiological HealthCompliance: Devices
July 27, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
December 8, 2017Not classifiedNew England District Office
March 13, 2017NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
November 21, 2014VAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
View all 9 other inspections on the company page
Other documents for Cynosure, Llc
  • FDA Inspection 1295506 - 2025-12-12
  • FDA Inspection 1060207 - 2018-07-27
  • FDA Inspection 1051787 - 2017-12-08
  • FDA Inspection 1003091 - 2017-03-13
  • FDA Inspection 904967 - 2014-11-21

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