# FDA 483 - Liveyon - September 21, 2018

Source: https://www.globalkeysolutions.net/records/483/liveyon/ba5efb70-906d-4ded-8666-5dc55a0df63a

> FDA 483 for Liveyon on September 21, 2018. Product: Devices. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Liveyon
- Inspection Date: 2018-09-21
- Product Type: Devices
- Office Name: Los Angeles District Office

## Related Documents

- [483 - 2019-05-23](https://www.globalkeysolutions.net/records/483/liveyon/0aa41747-5445-4f02-9ddf-15f7260d4837)

## Related Officers

- [Recall Coordinator](https://www.globalkeysolutions.net/people/thanh-b-tran/19f057a0-bb62-4d05-b79c-073e24be6480)
- [Tania Y. Hall](https://www.globalkeysolutions.net/people/tania-y-hall/94f342b2-a5f3-4ff1-ae5a-7f75fefe2214)

Company: https://www.globalkeysolutions.net/companies/liveyon/668e46df-24a9-4a18-baf6-9d0752315ec0

Office: https://www.globalkeysolutions.net/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b