# Bruker Daltonics, Inc. – FDA Inspection, Apr 1, 2016

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

> FDA inspection 964861 of Bruker Daltonics, Inc., April 01, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 820 and 1002. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 964861
- Company Name: Bruker Daltonics, Inc.
- Inspection Date: 2016-04-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1054427 - 2018-05-18](https://www.keypedia.com/records/fda_inspections/bruker-daltonics-inc/a7b38b1b-d9f4-4e47-b2c4-cf50ff1a667c)

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