# FDA Inspection 1097763 - Synedgen Inc. - July 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/synedgen-inc/a3ac786a-b6a1-4e02-a028-fac8fb0b4ccf
Source feed: FDA_Inspections

> FDA Inspection 1097763 for Synedgen Inc. on July 26, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1097763
- Company Name: Synedgen Inc.
- Inspection Date: 2019-07-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1097763 - 2019-07-26](https://www.keypedia.com/records/fda_inspections/synedgen-inc/d3da6f07-7c93-4062-b0e4-7111450d4c45)

Company: https://www.keypedia.com/companies/synedgen-inc/a1d04c3b-ea1c-4d03-a484-5cd727c38e34

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