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FDA Inspection
•Ellis Ophthalmic Technologies, Inc.•January 26, 2011

Ellis Ophthalmic Technologies, Inc. – FDA Inspection, Jan 26, 2011

Record Details

This FDA Inspection record concerns Ellis Ophthalmic Technologies, Inc., with an inspection on January 26, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Ellis Ophthalmic Technologies, Inc.
Inspection Date
January 26, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · cebbe20c-fadb-4e09-a67e-f90e9977fb24

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
708147
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
October 25, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
February 18, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
January 8, 2013VAICenter 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 1070574 - 2018-10-25
  • FDA Inspection 915089 - 2015-02-18
  • FDA Inspection 813406 - 2013-01-08
  • FDA Inspection 556629 - 2008-12-11

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