# Sofregen Medical Inc. – FDA Inspection, Jul 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/sofregen-medical-inc/6e3a69fa-b82b-4d9a-bff5-d6b243155863
Source feed: FDA_Inspections

> FDA inspection 1098102 of Sofregen Medical Inc., July 31, 2019. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098102
- Company Name: Sofregen Medical Inc.
- Inspection Date: 2019-07-31
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sara-m-onyango/643c6ad3-9747-4bc2-9e8e-72f97b11e659)

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

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