# Cerner Enviza LLC – FDA Inspection, Jun 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/cerner-enviza-llc/9a1e8d3f-218d-4c65-b441-865c86f2508f
Source feed: FDA_Inspections

> FDA inspection 1015239 of Cerner Enviza LLC, June 21, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015239
- Company Name: Cerner Enviza LLC
- Inspection Date: 2017-06-21
- 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: 0

## Related Documents

- FDA Inspection 1122961 - 2018-09-18
- FDA Inspection 880256 - 2014-05-30
- FDA Inspection 667664 - 2010-06-01

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)
- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

Company: https://www.keypedia.com/companies/cerner-enviza-llc/fe45d745-5dc1-4f53-82fc-0eed751c2ecd

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