# Eden Spine Europe, SA – FDA Inspection, Feb 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/eden-spine-europe-sa/b3f0b0e5-8c6b-40f8-abfe-352d9596bd02
Source feed: FDA_Inspections

> FDA inspection 1006424 of Eden Spine Europe, SA, February 10, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006424
- Company Name: Eden Spine Europe, SA
- Inspection Date: 2017-02-10
- 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: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/james-d-hildreth/1fb2f65a-9905-4848-83a3-16cb1f9e2179)

Company: https://www.keypedia.com/companies/eden-spine-europe-sa/bc22a0e6-a732-4362-8378-c156aa156376

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