# FDA Inspection 1023290 - Soterix Medical, Inc. - August 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/soterix-medical-inc/4910a143-9d8e-4a31-a794-5ce960e468f1
Source feed: FDA_Inspections

> FDA Inspection 1023290 for Soterix Medical, Inc. on August 24, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1023290
- Company Name: Soterix Medical, Inc.
- Inspection Date: 2017-08-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/soterix-medical-inc/a7eb1261-0277-49dc-8b26-c446fc69aac6

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