# Soterix Medical, Inc. – FDA Inspection, Aug 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 of Soterix Medical, Inc., August 24, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023290
- Company Name: Soterix Medical, Inc.
- Inspection Date: 2017-08-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1122115 - 2018-09-19](https://www.keypedia.com/records/fda_inspections/soterix-medical-inc/998a4810-d8ff-4e11-a299-990b1f6c39e9)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

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