FDA Inspection 1028860 - Beckman Coulter, Inc. - October 16, 2017

FDA Inspection 1028860 for Beckman Coulter, Inc. on October 16, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1028860 for Beckman Coulter, Inc. on October 16, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.198(c)

21 CFR 820.200(a)

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Record Information

Company

Beckman Coulter, Inc.

Inspection Date

October 16, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ffe0945c-0305-4021-b39c-80f216e955a4

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