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FDA Inspection
•Jardon Eye Prosthetics, Inc.•December 12, 2013

Jardon Eye Prosthetics, Inc. – FDA Inspection, Dec 12, 2013

Record Details

This FDA Inspection record concerns Jardon Eye Prosthetics, Inc., with an inspection on December 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Jardon Eye Prosthetics, Inc.
Inspection Date
December 12, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · bfb6e66d-3438-4693-863d-d2ea1275684a

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
858542
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Jardon Eye Prosthetics, Inc.

5
DateClassificationOfficeProject area
March 2, 2026NAIDetroit District OfficePostmarket Assurance: Medical Devices
August 31, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
October 7, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
June 16, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
April 30, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Jardon Eye Prosthetics, Inc.
  • FDA Inspection 1305052 - 2026-03-02
  • FDA Inspection 1024335 - 2017-08-31
  • FDA Inspection 748664 - 2011-10-07
  • FDA Inspection 666773 - 2010-06-16
  • FDA Inspection 580924 - 2009-04-30

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