# Bruker Daltronics – FDA Inspection, Oct 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/bruker-daltronics/8dd15473-cc58-402a-8831-2169a76cb79e
Source feed: FDA_Inspections

> FDA inspection 1069501 of Bruker Daltronics, October 18, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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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)
- 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: 3

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jeffrey-j-thibodeau/62b74030-4aef-400b-8ae2-8bf84712d813)

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