# FDA Inspection 696735 - NIOX Inc - November 05, 2010

Source: https://www.keypedia.com/records/fda_inspections/niox-inc/cc9115c1-405a-4562-bdf4-7efa281c1e3b
Source feed: FDA_Inspections

> FDA Inspection 696735 for NIOX Inc on November 05, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 696735
- Company Name: NIOX Inc
- Inspection Date: 2010-11-05
- 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/niox-inc/11ea0c1f-a68b-4834-a1ad-d0866a4b6816

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