# FDA Inspection 1267821 - Silony Spine Corporation - April 03, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/silony-spine-corporation/daa3f948-49de-4271-a6a2-a70e8805aca3
Source feed: FDA_Inspections

> FDA Inspection 1267821 for Silony Spine Corporation on April 03, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1267821
- Company Name: Silony Spine Corporation
- Inspection Date: 2025-04-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1267821 - 2025-04-03](https://www.globalkeysolutions.net/records/fda_inspections/silony-spine-corporation/3f49d136-5726-4de0-8657-bdef890aebb4)
- [FDA Inspection 1267821 - 2025-04-03](https://www.globalkeysolutions.net/records/fda_inspections/silony-spine-corporation/ead14f79-e535-40c4-a370-268a5a577cf0)

Company: https://www.globalkeysolutions.net/companies/silony-spine-corporation/f494a48b-5a01-49b7-8ffa-639607ef0c4e

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