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FDA Inspection
•Unitron Hearing Inc•April 4, 2017

Unitron Hearing Inc – FDA Inspection, Apr 4, 2017

Record Details

This FDA Inspection record concerns Unitron Hearing Inc, with an inspection on April 4, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Unitron Hearing Inc
Inspection Date
April 4, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Joseph D. Gong (Company Rep)
View Company Profile

ID · c6767669-5f4a-4ffa-8d1c-2e4a2d049217

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1012389
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Unitron Hearing Inc

2
DateClassificationOfficeProject area
January 12, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
December 3, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Unitron Hearing Inc
  • FDA Inspection 977966 - 2016-01-12
  • FDA Inspection 632332 - 2009-12-03

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