# FDA Inspection 1010441 - Medi Bayreuth - April 05, 2017

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

> FDA Inspection 1010441 for Medi Bayreuth on April 05, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010441
- Company Name: Medi Bayreuth
- Inspection Date: 2017-04-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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