# FDA Inspection 1003090 - Beckman Coulter GmbH - February 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/beckman-coulter-gmbh/1adc7700-f7e1-45e0-9c8a-929b44714950
Source feed: FDA_Inspections

> FDA Inspection 1003090 for Beckman Coulter GmbH on February 02, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003090
- Company Name: Beckman Coulter GmbH
- Inspection Date: 2017-02-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/beckman-coulter-gmbh/bcfa4034-16b9-4929-9d03-d10992ac608b

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