# Kreyenberg Gmbh – FDA Inspection, 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 of Kreyenberg Gmbh, May 11, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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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)
- 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: 3

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/claudette-d-brooks/10f30b8f-2d20-4f92-84c1-862b31b81ce1)

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