# FDA Inspection 791823 - Beckman Coulter, Inc. - July 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/beckman-coulter-inc/c7ffc015-282d-4b02-bae4-65149eec0b84
Source feed: FDA_Inspections

> FDA Inspection 791823 for Beckman Coulter, Inc. on July 20, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791823
- Company Name: Beckman Coulter, Inc.
- Inspection Date: 2012-07-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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