# FDA Inspection 669650 - Theken Spine LLC - July 02, 2010

Source: https://www.keypedia.com/records/fda_inspections/theken-spine-llc/99c6764a-cfa6-45dc-98d1-a340de6326d9
Source feed: FDA_Inspections

> FDA Inspection 669650 for Theken Spine LLC on July 02, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 669650
- Company Name: Theken Spine LLC
- Inspection Date: 2010-07-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 790400 - 2012-07-12](https://www.keypedia.com/records/fda_inspections/theken-spine-llc/9673a606-f520-4c0f-a142-9996f96cd53c)
- [FDA Inspection 790400 - 2012-07-12](https://www.keypedia.com/records/fda_inspections/theken-spine-llc/2b9c3e6b-fcb2-43ea-971d-1c6125d12834)

Company: https://www.keypedia.com/companies/theken-spine-llc/e1037585-9953-449b-a79c-a5f7775faff7

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