# Silq Technologies Corporation – FDA Inspection, Jan 5, 2023

Source: https://www.keypedia.com/records/fda_inspections/silq-technologies-corporation/b05be1b7-abe5-4029-8ffb-e0abdf3bd87e
Source feed: FDA_Inspections

> FDA inspection 1194223 of Silq Technologies Corporation, January 05, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1194223
- Company Name: Silq Technologies Corporation
- Inspection Date: 2023-01-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1287360 - 2025-10-16](https://www.keypedia.com/records/fda_inspections/silq-technologies-corporation/3e94f153-a8d2-435c-895b-55ca92abdaee)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/ronald-ifraimov/b4ce8b79-3fa2-4862-b7a4-68e14e45d87a)

Company: https://www.keypedia.com/companies/silq-technologies-corporation/51a857e2-de03-480e-b71d-c5273fb48e1e

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