# Aurident Inc – FDA Inspection, Oct 15, 2026

Source: https://www.keypedia.com/records/fda_inspections/aurident-inc/50dc2fba-1ae7-4957-9700-6aeac9810417
Source feed: FDA_Inspections

> FDA inspection 1341670 of Aurident Inc, October 15, 2026. Classification: Voluntary Action Indicated (VAI). 3 citations. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1341670
- Company Name: Aurident Inc
- Inspection Date: 2026-10-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1067019 - 2018-09-27](https://www.keypedia.com/records/fda_inspections/aurident-inc/ef8aaa1e-94be-4115-b2a7-e15b627b3e50)
- FDA Inspection 816456 - 2013-01-29
- FDA Inspection 761092 - 2011-12-07

Company: https://www.keypedia.com/companies/aurident-inc/498bd7dc-e80f-4ded-a3cf-4aef0103af22

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