# Tontarra Medizintechnik Gmbh – FDA Inspection, Jun 9, 2016

Source: https://www.keypedia.com/records/fda_inspections/tontarra-medizintechnik-gmbh/6ea746a4-2aad-4767-8ea6-90488d08fc97
Source feed: FDA_Inspections

> FDA inspection 976324 of Tontarra Medizintechnik Gmbh, June 09, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 976324
- Company Name: Tontarra Medizintechnik Gmbh
- Inspection Date: 2016-06-09
- 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: 3

## Related Documents

- FDA Inspection 1077626 - 2018-12-06
- [FDA Inspection 873811 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/tontarra-medizintechnik-gmbh/c0d9df4c-fd41-437b-89cc-4bbb5637a582)

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