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FDA Inspection
•Aurora Optics Company Inc.•October 17, 2014

Aurora Optics Company Inc. – FDA Inspection, Oct 17, 2014

Record Details

This FDA Inspection record concerns Aurora Optics Company Inc., with an inspection on October 17, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Aurora Optics Company Inc.
Inspection Date
October 17, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 59a7a42d-fcfe-4347-9828-1de11045dee1

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
900651
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Aurora Optics Company Inc.

3
DateClassificationOfficeProject area
November 4, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
February 10, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
October 16, 2012OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Aurora Optics Company Inc.
  • FDA Inspection 992377 - 2016-11-04
  • FDA Inspection 963211 - 2016-02-10
  • FDA Inspection 803869 - 2012-10-16

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