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FDA Inspection
•EyeKon Medical, Inc.•October 3, 2008

EyeKon Medical, Inc. – FDA Inspection, Oct 3, 2008

Record Details

This FDA Inspection record concerns EyeKon Medical, Inc., with an inspection on October 3, 2008, issued by the Center for Devices and Radiological Health, covering devices.

Company
EyeKon Medical, Inc.
Inspection Date
October 3, 2008
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 35445e0c-f956-4717-b2e3-ec0674699ceb

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
540097
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of EyeKon Medical, Inc.

4
DateClassificationOfficeProject area
June 10, 2025NAIFlorida District OfficePostmarket Assurance: Medical Devices
February 16, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 28, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 12, 2009NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for EyeKon Medical, Inc.
  • FDA Inspection 1251720 - 2025-06-10
  • FDA Inspection 1042012 - 2018-02-16
  • FDA Inspection 809132 - 2012-11-28
  • FDA Inspection 588902 - 2009-06-12

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