# Bricon Technology GmbH – FDA Inspection, Oct 17, 2019

Source: https://www.keypedia.com/records/fda_inspections/bricon-technology-gmbh/6ff6b34b-1ce4-49bc-b7f7-03f9d9e0d809
Source feed: FDA_Inspections

> FDA inspection 1109312 of Bricon Technology GmbH, October 17, 2019. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109312
- Company Name: Bricon Technology GmbH
- Inspection Date: 2019-10-17
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1003949 - 2017-02-02
- [FDA Inspection 867227 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/bricon-technology-gmbh/e45f4923-80dc-481c-8ca7-ecf33c1a0447)

Company: https://www.keypedia.com/companies/bricon-technology-gmbh/1f77cf14-5aeb-4768-9c2f-475f4a99c961

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