# FDA Inspection 1020251 - Kreyenberg Gmbh - May 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/kreyenberg-gmbh/856bb98f-2ecf-4bd2-a0c0-8d870911efca
Source feed: FDA_Inspections

> FDA Inspection 1020251 for Kreyenberg Gmbh on May 11, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020251
- Company Name: Kreyenberg Gmbh
- Inspection Date: 2017-05-11
- 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/kreyenberg-gmbh/af57a1b4-2ee2-469a-94bc-b4f64c1142f0

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