# FDA Inspection 1256478 - Ikonisys Inc. - December 10, 2024

Source: https://www.keypedia.com/records/fda_inspections/ikonisys-inc/037e0e35-242c-4e63-9a89-cbb992f0c08e
Source feed: FDA_Inspections

> FDA Inspection 1256478 for Ikonisys Inc. on December 10, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1256478
- Company Name: Ikonisys Inc.
- Inspection Date: 2024-12-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1256478 - 2024-12-10](https://www.keypedia.com/records/fda_inspections/ikonisys-inc/a730ab93-524f-4e2a-851a-bc32510b8814)
- [FDA Inspection 1256478 - 2024-12-10](https://www.keypedia.com/records/fda_inspections/ikonisys-inc/e2535002-56f1-498c-9976-43a318bb418b)
- [FDA Inspection 1256478 - 2024-12-10](https://www.keypedia.com/records/fda_inspections/ikonisys-inc/97dfc473-8e66-421e-9519-52d4a6f16d90)
- [FDA Inspection 1182197 - 2022-10-12](https://www.keypedia.com/records/fda_inspections/ikonisys-inc/b1077057-e6b0-45b7-99ec-aad6fa9aa20b)
- [FDA Inspection 1182197 - 2022-10-12](https://www.keypedia.com/records/fda_inspections/ikonisys-inc/836d24fd-5a22-4943-b0f5-5c45756fee8e)

Company: https://www.keypedia.com/companies/ikonisys-inc/d5f358f9-ef5e-42c9-9246-cbfabe9cf6ee

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