# FDA Inspection 1042884 - Precision Spine Inc - August 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/precision-spine-inc/0283b7bd-fc59-4f22-97d2-ac7a21c6f413
Source feed: FDA_Inspections

> FDA Inspection 1042884 for Precision Spine Inc on August 11, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042884
- Company Name: Precision Spine Inc
- Inspection Date: 2017-08-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1042884 - 2017-08-11](https://www.keypedia.com/records/fda_inspections/precision-spine-inc/3951e197-f278-4ded-b9b4-391940c2a04c)
- [FDA Inspection 919231 - 2015-03-18](https://www.keypedia.com/records/fda_inspections/precision-spine-inc/c2118224-3c9c-4bc4-810b-156c77a219a5)
- [FDA Inspection 709036 - 2011-02-01](https://www.keypedia.com/records/fda_inspections/precision-spine-inc/a6fbafd6-ea4e-45de-84f0-d5f67cca6bf0)

Company: https://www.keypedia.com/companies/precision-spine-inc/b00030e1-6c94-41bc-8ae1-30ea03d58f54

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