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FDA Inspection
•Geratherm Medical AG•December 19, 2013

Geratherm Medical AG – FDA Inspection, Dec 19, 2013

Record Details

This FDA Inspection record concerns Geratherm Medical AG, with an inspection on December 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Geratherm Medical AG
Inspection Date
December 19, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 280d8bc7-7ae6-4281-a27c-e005da22317f

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
860121
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 820.100(b)Documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Geratherm Medical AG

1
DateClassificationOfficeProject area
June 9, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Geratherm Medical AG
  • FDA Inspection 729812 - 2011-06-09

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