# Aurora Spine Inc – FDA Inspection, Sep 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/aurora-spine-inc/dee7aa3b-9b34-4b17-ad51-c4412bb345ee
Source feed: FDA_Inspections

> FDA inspection 1028588 of Aurora Spine Inc, September 18, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1028588
- Company Name: Aurora Spine Inc
- Inspection Date: 2017-09-18
- 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: 4

## Related Documents

- FDA Inspection 1063919 - 2018-07-30
- [FDA Inspection 881967 - 2014-05-23](https://www.keypedia.com/records/fda_inspections/aurora-spine-inc/ca9fb7e5-62ff-44fa-832c-0b4830e2dada)

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

Company: https://www.keypedia.com/companies/aurora-spine-inc/6cced3a5-bedd-4799-817d-422095631796

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