# FDA Inspection 1022883 - Inogen, Inc - August 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/inogen-inc/c7df525a-429c-4b0a-b8eb-4ac905b8abd0
Source feed: FDA_Inspections

> FDA Inspection 1022883 for Inogen, Inc on August 23, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022883
- Company Name: Inogen, Inc
- Inspection Date: 2017-08-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 837168 - 2013-06-26](https://www.keypedia.com/records/fda_inspections/inogen-inc/d37c0c8d-c4d3-4c16-8a7f-def4bf2503d7)
- [FDA Inspection 837168 - 2013-06-26](https://www.keypedia.com/records/fda_inspections/inogen-inc/68096f61-2754-4fbf-89b3-29da9e27f75b)

Company: https://www.keypedia.com/companies/inogen-inc/058b6461-ebda-4f36-af05-7b84a8efa0b3

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