FDA Inspection 1064813 - CareFusion 303, Inc. - September 06, 2018

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Record Details

This FDA Inspection record concerns CareFusion 303, Inc., with an inspection on September 6, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: CareFusion 303, Inc.
Inspection Date: September 6, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 21cd551f-a6f2-4cc8-8e02-e7aa779bcb8e

Violation Codes3

21 CFR 820.100(a)21 CFR 820.198(c)21 CFR 820.30(f)

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