# East West Wisconsin – FDA Inspection, Jun 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/east-west-wisconsin/eb3a74a1-8afe-4e82-886d-23869b21a55c
Source feed: FDA_Inspections

> FDA inspection 1017482 of East West Wisconsin, June 15, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations 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: 1017482
- Company Name: East West Wisconsin
- Inspection Date: 2017-06-15
- 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: 2

## Related Documents

- FDA Inspection 1251923 - 2024-09-26
- FDA Inspection 945304 - 2015-08-06

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michelle-j-glembin/e58f4652-d09f-41a7-941d-335c7b5338ad)
- [FDA Associated Person](https://www.keypedia.com/people/ross-j-grigsby/713f8252-3e41-4e6f-abea-8ca5bd48aa83)

Company: https://www.keypedia.com/companies/east-west-wisconsin/0b11fa50-6474-4e47-bfde-c4ae6eadc8ae

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