# FDA Inspection 992377 - Aurora Optics Company Inc. - November 04, 2016

Source: https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/68c7fb63-9d74-484d-8eb3-5c52dc3ce27d
Source feed: FDA_Inspections

> FDA Inspection 992377 for Aurora Optics Company Inc. on November 04, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992377
- Company Name: Aurora Optics Company Inc.
- Inspection Date: 2016-11-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## 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](https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/35e85508-0b2b-4840-95e2-d1cb6bc4713c)
- [FDA Inspection 963211 - 2016-02-10](https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/2c78a9e3-ce6c-4140-b573-4265d27588ea)
- [FDA Inspection 900651 - 2014-10-17](https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/59a7a42d-fcfe-4347-9828-1de11045dee1)
- [FDA Inspection 900651 - 2014-10-17](https://www.keypedia.com/records/fda_inspections/aurora-optics-company-inc/58800e20-fc54-4355-be8a-cd803e0c96aa)

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