# FDA Inspection 986634 - NIOX Inc - August 04, 2016

Source: https://www.keypedia.com/records/fda_inspections/niox-inc/47706a6a-82f6-4af6-9dee-90f6bee45e42
Source feed: FDA_Inspections

> FDA Inspection 986634 for NIOX Inc on August 04, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 986634
- Company Name: NIOX Inc
- Inspection Date: 2016-08-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 986634 - 2016-08-04](https://www.keypedia.com/records/fda_inspections/niox-inc/78ba976c-870c-4555-ae4a-50bb679d987f)
- [FDA Inspection 696735 - 2010-11-05](https://www.keypedia.com/records/fda_inspections/niox-inc/cc9115c1-405a-4562-bdf4-7efa281c1e3b)
- [FDA Inspection 696735 - 2010-11-05](https://www.keypedia.com/records/fda_inspections/niox-inc/898f12fd-50b4-469e-91b4-d9273e5908a1)

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