# FDA Inspection 993878 - Aionex, Inc. - December 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/aionex-inc/20e2fb2b-fdc4-4d2d-b956-c23d1dc186cc
Source feed: FDA_Inspections

> FDA Inspection 993878 for Aionex, Inc. on December 02, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993878
- Company Name: Aionex, Inc.
- Inspection Date: 2016-12-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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