# FDA Inspection 1234783 - Kenex (Electro-Medical) Ltd. - March 14, 2024

Source: https://www.keypedia.com/records/fda_inspections/kenex-electro-medical-ltd/5ac2afed-7d5e-42f0-ba93-210086a9edcd
Source feed: FDA_Inspections

> FDA Inspection 1234783 for Kenex (Electro-Medical) Ltd. on March 14, 2024. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1234783
- Company Name: Kenex (Electro-Medical) Ltd.
- Inspection Date: 2024-03-14
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234783 - 2024-03-14](https://www.keypedia.com/records/fda_inspections/kenex-electro-medical-ltd/3d63a102-1736-4a5f-8182-09c389b32965)

Company: https://www.keypedia.com/companies/kenex-electro-medical-ltd/1b979611-c01d-4e9e-888f-790122d8b45f

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