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FDA Inspection
•Ellis Ophthalmic Technologies, Inc.•October 25, 2018

Ellis Ophthalmic Technologies, Inc. – FDA Inspection, Oct 25, 2018

Record Details

This FDA Inspection record concerns Ellis Ophthalmic Technologies, Inc., with an inspection on October 25, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Ellis Ophthalmic Technologies, Inc.
Inspection Date
October 25, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Kwong P. Lee (Company Rep)
  • Preston M. Lee (Investigator)
View Company Profile

ID · c7dc205c-f7d3-42c7-b09e-eb9f8c8f7fba

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1070574
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Ellis Ophthalmic Technologies, Inc.

5
DateClassificationOfficeProject area
November 4, 2022NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 18, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
January 8, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
January 26, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
December 11, 2008NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Ellis Ophthalmic Technologies, Inc.
  • FDA Inspection 1190599 - 2022-11-04
  • FDA Inspection 915089 - 2015-02-18
  • FDA Inspection 813406 - 2013-01-08
  • FDA Inspection 708147 - 2011-01-26
  • FDA Inspection 556629 - 2008-12-11

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