FDA Inspection 1199006 - US Infusion, Inc. - March 06, 2023

FDA Inspection 1199006 for US Infusion, Inc. on March 06, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1199006 for US Infusion, Inc. on March 06, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(b)

21 CFR 820.50(a)

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Record Information

Company

US Infusion, Inc.

Inspection Date

March 6, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8830d86-def1-4d95-9d01-30313ef9fa56

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