# FDA Inspection 961776 - Beckman Coulter, Inc. - January 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/beckman-coulter-inc/acd2da8d-57d6-4e2a-9fa0-36a3a36d683e
Source feed: FDA_Inspections

> FDA Inspection 961776 for Beckman Coulter, Inc. on January 27, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 961776
- Company Name: Beckman Coulter, Inc.
- Inspection Date: 2016-01-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 961776 - 2016-01-27](https://www.keypedia.com/records/fda_inspections/beckman-coulter-inc/8c49dadf-25aa-4853-baed-a1deabdcd18a)
- [FDA Inspection 791823 - 2012-07-20](https://www.keypedia.com/records/fda_inspections/beckman-coulter-inc/9a07a203-a1f0-4f7a-871f-76e6a0f6a9ef)
- [FDA Inspection 791823 - 2012-07-20](https://www.keypedia.com/records/fda_inspections/beckman-coulter-inc/c7ffc015-282d-4b02-bae4-65149eec0b84)

Company: https://www.keypedia.com/companies/beckman-coulter-inc/43922b92-4f61-4aa5-aeec-a4041582a1f5

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