# FDA Inspection 1098102 - Sofregen Medical Inc. - July 31, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/sofregen-medical-inc/33b27e9e-813c-42df-b7b4-162f4d07899f
Source feed: FDA_Inspections

> FDA Inspection 1098102 for Sofregen Medical Inc. on July 31, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098102
- Company Name: Sofregen Medical Inc.
- Inspection Date: 2019-07-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1098102 - 2019-07-31](https://www.globalkeysolutions.net/records/fda_inspections/sofregen-medical-inc/6e3a69fa-b82b-4d9a-bff5-d6b243155863)

Company: https://www.globalkeysolutions.net/companies/sofregen-medical-inc/b316723d-d2ba-4433-9edc-d6cf709bee77

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