FDA EIR - Beckman Coulter Inc. - October 30, 2019

FDA EIR for Beckman Coulter Inc. on October 30, 2019. Product: devices. Access full analysis and detailed observations.

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Record Summary

FDA EIR for Beckman Coulter Inc. on October 30, 2019. Product: devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.198

21 CFR 820.30

21 CFR 820.100

21 CFR 803

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Record Information

Company

Beckman Coulter Inc.

Inspection Date

October 30, 2019

Product Type

devices

Office

Office of Medical Device and Radiological Health Operations, Division 3 – West

People

ID: 97c9463d-66fa-4c26-a4c4-33529e38d676

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