# Endologix, Inc. – FDA Inspection, May 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/endologix-inc/a7159e94-6fbe-407c-9a82-c7edfbabd7e6
Source feed: FDA_Inspections

> FDA inspection 1091013 of Endologix, Inc., May 24, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091013
- Company Name: Endologix, Inc.
- Inspection Date: 2019-05-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/thea-c-grome/ff1a4a19-f74c-485a-a177-f4cc5c5b7499)

Company: https://www.keypedia.com/companies/endologix-inc/7522f1d0-6e55-4771-b06a-b7ed741cedbf

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