# Aurident Inc – FDA Inspection, Sep 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/aurident-inc/ef8aaa1e-94be-4115-b2a7-e15b627b3e50
Source feed: FDA_Inspections

> FDA inspection 1067019 of Aurident Inc, September 27, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1067019
- Company Name: Aurident Inc
- Inspection Date: 2018-09-27
- 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: 2

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- FDA Inspection 816456 - 2013-01-29
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## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

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