# Jeio Tech Inc. – FDA Inspection, May 2, 2018

Source: https://www.keypedia.com/records/fda_inspections/jeio-tech-inc/7dbf9d6d-ea09-4233-8503-bbb7810f7e8f
Source feed: FDA_Inspections

> FDA inspection 1050716 of Jeio Tech Inc., May 02, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

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