# Geratherm Medical AG – FDA Inspection, Dec 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 of Geratherm Medical AG, December 19, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- 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: 1

## Related Documents

- FDA Inspection 729812 - 2011-06-09

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