# FDA Inspection 964861 - Bruker Daltonics, Inc. - April 01, 2016

Source: https://www.keypedia.com/records/fda_inspections/bruker-daltonics-inc/4aeaaab8-df4e-42db-b1cb-80c2f39fda23
Source feed: FDA_Inspections

> FDA Inspection 964861 for Bruker Daltonics, Inc. on April 01, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 964861
- Company Name: Bruker Daltonics, Inc.
- Inspection Date: 2016-04-01
- 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 1054427 - 2018-05-18](https://www.keypedia.com/records/fda_inspections/bruker-daltonics-inc/a7b38b1b-d9f4-4e47-b2c4-cf50ff1a667c)
- [FDA Inspection 1054427 - 2018-05-18](https://www.keypedia.com/records/fda_inspections/bruker-daltonics-inc/6160b0bb-f4d2-441d-b35a-64b2aba2f7f5)
- [FDA Inspection 964861 - 2016-04-01](https://www.keypedia.com/records/fda_inspections/bruker-daltonics-inc/0103e5dd-8fb6-4a0f-9639-6c02f64ff27f)

Company: https://www.keypedia.com/companies/bruker-daltonics-inc/7ea3f57a-bd56-43c8-89d4-3e71d7f7bb59

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