# FDA Inspection 817588 - Rubimed AG - January 29, 2013

Source: https://www.keypedia.com/records/fda_inspections/rubimed-ag/25d0daa7-7fec-4abe-9421-c586ec5a01e9
Source feed: FDA_Inspections

> FDA Inspection 817588 for Rubimed AG on January 29, 2013. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817588
- Company Name: Rubimed AG
- Inspection Date: 2013-01-29
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 817588 - 2013-01-29](https://www.keypedia.com/records/fda_inspections/rubimed-ag/7a249a6b-dd2a-474c-88a2-50c5d4fe31ee)

Company: https://www.keypedia.com/companies/rubimed-ag/38dffe9f-e46b-411b-b273-bb3df22db7c2

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