# Aionex, Inc. – FDA Inspection, Nov 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/aionex-inc/d8cb82c9-055d-4766-9ba2-7dd427b150f3
Source feed: FDA_Inspections

> FDA inspection 808865 of Aionex, Inc., November 20, 2012. Classification: Official Action Indicated (OAI). 12 citations under 21 CFR parts 803 and 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 808865
- Company Name: Aionex, Inc.
- Inspection Date: 2012-11-20
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

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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