# FDA Inspection 1035423 - TherOx, Inc. - November 29, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/therox-inc/fa2a7a49-fdd2-4f7e-a070-cae8154142fb/
Source feed: FDA_Inspections

> FDA Inspection 1035423 for TherOx, Inc. on November 29, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035423
- Company Name: TherOx, Inc.
- Inspection Date: 2017-11-29
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/therox-inc/bc3214c3-8577-4fe0-913f-7ada32ceebed

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