# FDA Inspection 1049540 - ETI GmbH Ingenieurburo fur Medizintechnik - April 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/eti-gmbh-ingenieurburo-fur-medizintechnik/93e56172-9bd4-4e86-8552-5e32d00a5fad
Source feed: FDA_Inspections

> FDA Inspection 1049540 for ETI GmbH Ingenieurburo fur Medizintechnik on April 19, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1049540
- Company Name: ETI GmbH Ingenieurburo fur Medizintechnik
- Inspection Date: 2018-04-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/eti-gmbh-ingenieurburo-fur-medizintechnik/ee356fd3-ed7b-4b51-8339-12ac304ca34a

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