# Medi Bayreuth – FDA Inspection, Apr 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/medi-bayreuth/464df21f-800c-48a8-b5f9-e0a5b88ac542
Source feed: FDA_Inspections

> FDA inspection 1010441 of Medi Bayreuth, April 05, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1010441
- Company Name: Medi Bayreuth
- Inspection Date: 2017-04-05
- 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: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/elizabeth-d-connell/085f2b40-dcf8-40ad-ba33-d0970228768b)

Company: https://www.keypedia.com/companies/medi-bayreuth/c3f89fa8-f72d-4141-865b-3add5434fe3a

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