Hospira Inc.July 13, 2012

FDA 483 - Hospira Inc. - July 13, 2012

FDA 483 for Hospira Inc. on July 13, 2012. Product: N/A. Access full analysis and detailed observations.

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Record Summary

FDA 483 for Hospira Inc. on July 13, 2012. Product: N/A. Access full analysis and detailed observations.

Violation Codes

21 CFR 801

FD&C Act 801(a)(3)

21 CFR 820.75

21 CFR 820.198

21 CFR 820

21 CFR 820.100

21 CFR 820.40

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Record Information

Company

Hospira Inc.

Inspection Date

July 13, 2012

Product Type

Office

Chicago District Office

People

Jesse A. Vazquez (Medical Device Specialist)

ID: 11f2e46f-2756-4b6e-a8b0-104f23b3f5ac

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