# FDA Inspection 860797 - Sutter Medizintechnik GmbH - December 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/sutter-medizintechnik-gmbh/321b21d3-8009-4c51-a288-07e24b75613c
Source feed: FDA_Inspections

> FDA Inspection 860797 for Sutter Medizintechnik GmbH on December 12, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860797
- Company Name: Sutter Medizintechnik GmbH
- Inspection Date: 2013-12-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1029697 - 2017-09-28](https://www.keypedia.com/records/fda_inspections/sutter-medizintechnik-gmbh/d63d6e7f-1e6a-42e8-8d12-4da7f60379be)
- [FDA Inspection 860797 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/sutter-medizintechnik-gmbh/765cb15b-5d10-4b55-8ea8-13c4ec5ab424)

Company: https://www.keypedia.com/companies/sutter-medizintechnik-gmbh/b18f6c72-ed3e-4cab-a28e-fd885feee906

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