FDA Inspection 926924 - Carefusion 2200 Inc - May 07, 2015

FDA Inspection 926924 for Carefusion 2200 Inc on May 07, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 926924 for Carefusion 2200 Inc on May 07, 2015. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(b)

21 CFR 820.30(e)

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Record Information

Company

Carefusion 2200 Inc

Inspection Date

May 7, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb6648d8-c67f-45f8-80ab-b0f091c80257

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