# SPINEART SA – FDA Inspection, Sep 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/spineart-sa/1abde849-42ef-4a52-a5ec-0f1aa31d1b8c
Source feed: FDA_Inspections

> FDA inspection 852552 of SPINEART SA, September 10, 2013. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 852552
- Company Name: SPINEART SA
- Inspection Date: 2013-09-10
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1096341 - 2019-05-22
- FDA Inspection 996791 - 2016-12-08

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