# FDA Inspection 931994 - Fritz Huber Medizintechnik - June 25, 2015

Source: https://www.keypedia.com/records/fda_inspections/fritz-huber-medizintechnik/ac3926cc-9556-4228-a1e6-f4fc08f808cb
Source feed: FDA_Inspections

> FDA Inspection 931994 for Fritz Huber Medizintechnik on June 25, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 931994
- Company Name: Fritz Huber Medizintechnik
- Inspection Date: 2015-06-25
- 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 931994 - 2015-06-25](https://www.keypedia.com/records/fda_inspections/fritz-huber-medizintechnik/571fa4a1-13b0-4aec-a1e9-35c6fd3ab802)

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