# FDA Inspection 873811 - Tontarra Medizintechnik Gmbh - March 27, 2014

Source: https://www.keypedia.com/records/fda_inspections/tontarra-medizintechnik-gmbh/2b66af79-2064-47f0-957f-598bdf50adcb
Source feed: FDA_Inspections

> FDA Inspection 873811 for Tontarra Medizintechnik Gmbh on March 27, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 873811
- Company Name: Tontarra Medizintechnik Gmbh
- Inspection Date: 2014-03-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/tontarra-medizintechnik-gmbh/bb9d5884-7789-4db6-94f2-1f9ae1d65609

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