# ETI GmbH Ingenieurburo fur Medizintechnik – FDA Inspection, Apr 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 of ETI GmbH Ingenieurburo fur Medizintechnik, April 19, 2018. Classification: Voluntary Action Indicated (VAI). 11 citations under 21 CFR part 820. Form 483 issued.

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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)
- 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: 11

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/james-d-hildreth/1fb2f65a-9905-4848-83a3-16cb1f9e2179)

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