# FDA Inspection 1050716 - Jeio Tech Inc. - May 02, 2018

Source: https://www.keypedia.com/records/fda_inspections/jeio-tech-inc/345e126a-4698-487a-b40e-85b9e852bfb7
Source feed: FDA_Inspections

> FDA Inspection 1050716 for Jeio Tech Inc. on May 02, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050716
- Company Name: Jeio Tech Inc.
- Inspection Date: 2018-05-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1050716 - 2018-05-02](https://www.keypedia.com/records/fda_inspections/jeio-tech-inc/7dbf9d6d-ea09-4233-8503-bbb7810f7e8f)

Company: https://www.keypedia.com/companies/jeio-tech-inc/50215c43-97ff-4b73-932d-b0d0f51a45aa

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