# Inogen, Inc – FDA Inspection, Aug 23, 2017

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

> FDA inspection 1022883 of Inogen, Inc, August 23, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1127095 - 2018-09-27](https://www.keypedia.com/records/fda_inspections/inogen-inc/a9a18d07-24da-4f7b-be08-763268e00fe0)
- FDA Inspection 837168 - 2013-06-26

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jocelyn-c-turner/7e39f6e0-9750-4460-8a4e-27ee9306b77e)

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