# Aionex, Inc. – FDA Inspection, Jul 2, 2013

Source: https://www.keypedia.com/records/fda_inspections/aionex-inc/50eaf454-1230-45c9-9678-831c2679097d
Source feed: FDA_Inspections

> FDA inspection 838660 of Aionex, Inc., July 02, 2013. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 838660
- Company Name: Aionex, Inc.
- Inspection Date: 2013-07-02
- 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: 10

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- [FDA Inspection 808865 - 2012-11-20](https://www.keypedia.com/records/fda_inspections/aionex-inc/d8cb82c9-055d-4766-9ba2-7dd427b150f3)

Company: https://www.keypedia.com/companies/aionex-inc/1925159a-d28b-42ae-928e-f3ef139360dd

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