# FDA Inspection 1069501 - Bruker Daltronics - October 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/bruker-daltronics/3e85213e-e308-4195-bb31-2013f7ebfe0a
Source feed: FDA_Inspections

> FDA Inspection 1069501 for Bruker Daltronics on October 18, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069501
- Company Name: Bruker Daltronics
- Inspection Date: 2018-10-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1069501 - 2018-10-18](https://www.keypedia.com/records/fda_inspections/bruker-daltronics/8dd15473-cc58-402a-8831-2169a76cb79e)

Company: https://www.keypedia.com/companies/bruker-daltronics/9b27f10b-e19e-45bf-88d8-7c133ab2a5d0

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