# FDA Inspection 907300 - Vibracare Gmbh - December 18, 2014

Source: https://www.keypedia.com/records/fda_inspections/vibracare-gmbh/2d8ba1b2-8808-4744-b28c-d478f903921f
Source feed: FDA_Inspections

> FDA Inspection 907300 for Vibracare Gmbh on December 18, 2014. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 907300
- Company Name: Vibracare Gmbh
- Inspection Date: 2014-12-18
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 907300 - 2014-12-18](https://www.keypedia.com/records/fda_inspections/vibracare-gmbh/bf480017-ea66-4297-bcd1-b06969ca7e9d)

Company: https://www.keypedia.com/companies/vibracare-gmbh/f57451ab-746e-459c-ad02-a9e678e19fc4

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