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

Source: https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/59a7a42d-fcfe-4347-9828-1de11045dee1
Source feed: FDA_Inspections

> FDA inspection 900651 of Aurora Optics Company Inc., October 17, 2014. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900651
- Company Name: Aurora Optics Company Inc.
- Inspection Date: 2014-10-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 992377 - 2016-11-04](https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/7733d0a9-60b8-4207-8740-6972e358827d)
- FDA Inspection 963211 - 2016-02-10
- [FDA Inspection 803869 - 2012-10-16](https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/5d87683c-a6ed-47e7-a17c-3ee605cfd5ca)

Company: https://www.keypedia.com/companies/aurora-optics-company-inc/18151853-0b0c-460e-a5bd-a1a7ec8ee25f

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7