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FDA Inspection
•Candela Corporation•November 17, 2017

Candela Corporation – FDA Inspection, Nov 17, 2017

Record Details

This FDA Inspection record concerns Candela Corporation, with an inspection on November 17, 2017, issued by the New England District Office, covering medical devices & rad health.

Company
Candela Corporation
Inspection Date
November 17, 2017
Product Type
Medical Devices & Rad Health
Office
New England District Office
View Company Profile

ID · 8e00817b-1518-4280-9415-ff2975fd3c75

Inspection Facts

Inspection number
1048083
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Candela Corporation

3
DateClassificationOfficeProject area
February 8, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
February 21, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
October 18, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Candela Corporation
  • FDA Inspection 1002942 - 2017-02-08
  • FDA Inspection 868362 - 2014-02-21
  • FDA Inspection 752274 - 2011-10-18

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