# FDA Inspection 1228191 - Spinalight, Inc. - January 31, 2024

Source: https://www.keypedia.com/records/fda_inspections/spinalight-inc/27910548-928c-4bb6-9f4a-1562f04cfecc
Source feed: FDA_Inspections

> FDA Inspection 1228191 for Spinalight, Inc. on January 31, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1228191
- Company Name: Spinalight, Inc.
- Inspection Date: 2024-01-31
- 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 1228191 - 2024-01-31](https://www.keypedia.com/records/fda_inspections/spinalight-inc/3573e073-1eee-41f8-b710-8e591bdce569)
- [FDA Inspection 919385 - 2015-03-19](https://www.keypedia.com/records/fda_inspections/spinalight-inc/95daece1-69f4-49c8-ae67-d0fb0fa11c80)
- [FDA Inspection 919385 - 2015-03-19](https://www.keypedia.com/records/fda_inspections/spinalight-inc/032bda62-f2dc-4fc9-8f9e-73a63e05f6b8)
- [FDA Inspection 792598 - 2012-07-19](https://www.keypedia.com/records/fda_inspections/spinalight-inc/9ffb2255-3eae-4fb3-962d-3281958e4735)
- [FDA Inspection 792598 - 2012-07-19](https://www.keypedia.com/records/fda_inspections/spinalight-inc/4aa4267f-4be1-4fb8-98bf-da6803157de9)

Company: https://www.keypedia.com/companies/spinalight-inc/a41339f9-3026-4de3-822f-20d0e6a4fba2

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