# FDA Inspection 1191283 - Inogen, Inc - November 03, 2022

Source: https://www.keypedia.com/records/fda_inspections/inogen-inc/3cf648c6-fb1b-4ecc-b308-5df9acef7992
Source feed: FDA_Inspections

> FDA Inspection 1191283 for Inogen, Inc on November 03, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1191283
- Company Name: Inogen, Inc
- Inspection Date: 2022-11-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1191283 - 2022-11-03](https://www.keypedia.com/records/fda_inspections/inogen-inc/adb9df65-c456-407a-9c8c-caeeae434550)
- [FDA Inspection 965925 - 2016-03-03](https://www.keypedia.com/records/fda_inspections/inogen-inc/c4cab3c5-cf52-4678-ac44-5943f3b1086f)
- [FDA Inspection 875746 - 2014-04-17](https://www.keypedia.com/records/fda_inspections/inogen-inc/38a2715f-7f4c-42dd-bbbd-d7fdfc7b2588)
- [FDA Inspection 875746 - 2014-04-17](https://www.keypedia.com/records/fda_inspections/inogen-inc/39e83687-9a89-402e-aeb6-a53177cea124)
- [FDA Inspection 777057 - 2012-04-04](https://www.keypedia.com/records/fda_inspections/inogen-inc/7f4adf1d-ff4e-41a7-892f-7bed8735d206)

Company: https://www.keypedia.com/companies/inogen-inc/4b72c052-a43d-406c-adbc-cd1c3376cce3

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