# FDA Inspection 996791 - SPINEART SA - December 08, 2016

Source: https://www.keypedia.com/records/fda_inspections/spineart-sa/32c3096a-23ae-412c-9970-527ba6b8f503
Source feed: FDA_Inspections

> FDA Inspection 996791 for SPINEART SA on December 08, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 996791
- Company Name: SPINEART SA
- Inspection Date: 2016-12-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 852552 - 2013-09-10](https://www.keypedia.com/records/fda_inspections/spineart-sa/1abde849-42ef-4a52-a5ec-0f1aa31d1b8c)
- [FDA Inspection 852552 - 2013-09-10](https://www.keypedia.com/records/fda_inspections/spineart-sa/1bff6e0c-dedc-4a5f-a526-40b4e6af1d0d)

Company: https://www.keypedia.com/companies/spineart-sa/32cd7d45-9860-4578-826f-b2f3558cefeb

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