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FDA Inspection
•Westone Laboratories, Inc.•January 14, 2013

Westone Laboratories, Inc. – FDA Inspection, Jan 14, 2013

Record Details

This FDA Inspection record concerns Westone Laboratories, Inc., with an inspection on January 14, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Westone Laboratories, Inc.
Inspection Date
January 14, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 85adc80b-3e17-482a-8223-c744d3dc8b55

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
814099
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Westone Laboratories, Inc.

3
DateClassificationOfficeProject area
November 15, 2017VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 12, 2012OAICenter for Devices and Radiological HealthCompliance: Devices
April 6, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Westone Laboratories, Inc.
  • FDA Inspection 1031336 - 2017-11-15
  • FDA Inspection 790503 - 2012-07-12
  • FDA Inspection 579412 - 2009-04-06

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