# Fritz Huber Medizintechnik – FDA Inspection, Jan 29, 2020

Source: https://www.keypedia.com/records/fda_inspections/fritz-huber-medizintechnik/0eb94f1a-d757-493a-9bbb-215f20d37307
Source feed: FDA_Inspections

> FDA inspection 1116897 of Fritz Huber Medizintechnik, January 29, 2020. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1116897
- Company Name: Fritz Huber Medizintechnik
- Inspection Date: 2020-01-29
- 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: 1

## Related Documents

- [FDA Inspection 931994 - 2015-06-25](https://www.keypedia.com/records/fda_inspections/fritz-huber-medizintechnik/ac3926cc-9556-4228-a1e6-f4fc08f808cb)

Company: https://www.keypedia.com/companies/fritz-huber-medizintechnik/df9bc77a-22c4-4b86-8a7b-1c6bce4f761a

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