# FDA Inspection 849513 - Kyphon Sarl - September 20, 2013

Source: https://www.keypedia.com/records/fda_inspections/kyphon-sarl/85c47d5a-73a3-47c7-a3ca-19d2f3ba197c
Source feed: FDA_Inspections

> FDA Inspection 849513 for Kyphon Sarl on September 20, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 849513
- Company Name: Kyphon Sarl
- Inspection Date: 2013-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 849513 - 2013-09-20](https://www.keypedia.com/records/fda_inspections/kyphon-sarl/c65e860f-8a73-4a67-9740-a5b804de788b)
- [FDA Inspection 722979 - 2011-04-07](https://www.keypedia.com/records/fda_inspections/kyphon-sarl/4098e12c-d87d-4083-aabd-8d02cd908bac)

Company: https://www.keypedia.com/companies/kyphon-sarl/d29d191d-4954-4154-8a99-2b4c5058c393

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