# FDA Inspection 550670 - ROSE GMBH FUER MEDIZINTECHNIK - November 13, 2008

Source: https://www.keypedia.com/records/fda_inspections/rose-gmbh-fuer-medizintechnik/9d072d11-c30f-41f8-b4d3-cf54d8d8db5c
Source feed: FDA_Inspections

> FDA Inspection 550670 for ROSE GMBH FUER MEDIZINTECHNIK on November 13, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 550670
- Company Name: ROSE GMBH FUER MEDIZINTECHNIK
- Inspection Date: 2008-11-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 909925 - 2014-12-11](https://www.keypedia.com/records/fda_inspections/rose-gmbh-fuer-medizintechnik/67cac9cf-df3a-41e5-b2a9-60f701fe6a30)

Company: https://www.keypedia.com/companies/rose-gmbh-fuer-medizintechnik/cda5f8e5-471a-4561-b3ec-4aa9ec49bbcc

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