# FDA Inspection 777309 - SpineCraft, LLC. - April 12, 2012

Source: https://www.keypedia.com/records/fda_inspections/spinecraft-llc/4533d89b-ea5b-447c-a3f5-a4f7a98b2db2
Source feed: FDA_Inspections

> FDA Inspection 777309 for SpineCraft, LLC. on April 12, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 777309
- Company Name: SpineCraft, LLC.
- Inspection Date: 2012-04-12
- 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 1233747 - 2024-03-22](https://www.keypedia.com/records/fda_inspections/spinecraft-llc/9435c7d6-bd9c-43aa-81e4-7314d53bb8ca)
- [FDA Inspection 1074762 - 2018-12-13](https://www.keypedia.com/records/fda_inspections/spinecraft-llc/b78195fd-c293-4521-a425-235a56c418c0)
- [FDA Inspection 1074762 - 2018-12-13](https://www.keypedia.com/records/fda_inspections/spinecraft-llc/2d6f02fb-b149-4798-b49f-e95503cac528)
- [FDA Inspection 1073334 - 2018-11-14](https://www.keypedia.com/records/fda_inspections/spinecraft-llc/65645748-f01e-4e13-92ed-aeeecadebfce)
- [FDA Inspection 985974 - 2016-08-18](https://www.keypedia.com/records/fda_inspections/spinecraft-llc/61855d77-b600-4951-9372-25b9feb65f3a)

Company: https://www.keypedia.com/companies/spinecraft-llc/1f8afee0-4555-47a4-93df-1b10a279b5bc

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