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FDA Inspection
•Corentec Co., LTD•April 19, 2017

Corentec Co., LTD – FDA Inspection, Apr 19, 2017

Record Details

This FDA Inspection record concerns Corentec Co., LTD, with an inspection on April 19, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Corentec Co., LTD
Inspection Date
April 19, 2017
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Daniel J. Lahar (FDA Associated Person)
View Company Profile

ID · 2e5e6234-39d5-4d44-957d-1764bac3276a

Inspection Facts

Inspection number
1009769
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Corentec Co., LTD

4
DateClassificationOfficeProject area
August 29, 2024VAICenter for Devices and Radiological HealthCompliance: Devices
October 31, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
April 9, 2015VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 16, 2014VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Corentec Co., LTD
  • FDA Inspection 1243031 - 2024-08-29
  • FDA Inspection 1110015 - 2019-10-31
  • FDA Inspection 924849 - 2015-04-09
  • FDA Inspection 867451 - 2014-01-16

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