# Cerner Corporation, Innovation Campus – FDA Inspection, Jun 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/cerner-corporation-innovation-campus/34c2e834-4fa8-4948-a9a9-b21b5aa7ea80
Source feed: FDA_Inspections

> FDA inspection 1015240 of Cerner Corporation, Innovation Campus, June 21, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015240
- Company Name: Cerner Corporation, Innovation Campus
- Inspection Date: 2017-06-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1122110 - 2018-09-20](https://www.keypedia.com/records/fda_inspections/cerner-corporation-innovation-campus/216e930b-1d58-45bb-aee6-f9e2acc7718e)

## 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-corporation-innovation-campus/05693d91-6249-4287-a0b0-3cd9c353d3e8

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