# FDA Inspection 980035 - Spinal Simplicity LLC - July 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/spinal-simplicity-llc/0440ee6c-8cac-4d4c-9d4c-968cdd7ed44a
Source feed: FDA_Inspections

> FDA Inspection 980035 for Spinal Simplicity LLC on July 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980035
- Company Name: Spinal Simplicity LLC
- Inspection Date: 2016-07-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 980035 - 2016-07-20](https://www.keypedia.com/records/fda_inspections/spinal-simplicity-llc/1668fbef-7250-4aeb-930f-eb198b0b462d)
- [FDA Inspection 803612 - 2012-10-17](https://www.keypedia.com/records/fda_inspections/spinal-simplicity-llc/304808eb-2319-4165-adad-3e038f68db87)

Company: https://www.keypedia.com/companies/spinal-simplicity-llc/63e8449e-57ec-4790-810a-5328bb5ce10b

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