# FDA Inspection 1028588 - Aurora Spine Inc - September 18, 2017

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

> FDA Inspection 1028588 for Aurora Spine Inc on September 18, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028588
- Company Name: Aurora Spine Inc
- Inspection Date: 2017-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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