# FDA Inspection 860121 - Geratherm Medical AG - December 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/geratherm-medical-ag/280d8bc7-7ae6-4281-a27c-e005da22317f
Source feed: FDA_Inspections

> FDA Inspection 860121 for Geratherm Medical AG on December 19, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860121
- Company Name: Geratherm Medical AG
- Inspection Date: 2013-12-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 729812 - 2011-06-09](https://www.keypedia.com/records/fda_inspections/geratherm-medical-ag/2781f656-65fd-4657-999d-464f6d8d2b99)

Company: https://www.keypedia.com/companies/geratherm-medical-ag/b708a682-4659-41c7-9b1f-a4919d1b0f2a

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