# Vivonic GmbH – FDA Inspection, May 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/vivonic-gmbh/3b4aa7c2-7fe4-46aa-89a5-ebc1fbf3bb3a
Source feed: FDA_Inspections

> FDA inspection 1017154 of Vivonic GmbH, May 19, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017154
- Company Name: Vivonic GmbH
- Inspection Date: 2017-05-19
- 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: 5

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/vivonic-gmbh/9d2d5223-ed9d-4d3c-b181-2ef941ba71cf

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