FDA WARNING_LETTER - Hospira, Inc. - November 15, 2013

FDA WARNING_LETTER for Hospira, Inc. on November 15, 2013. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Hospira, Inc. on November 15, 2013. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.100(a)

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.198(a)

21 CFR 820.198(c)

21 U.S.C. 351(h)

21 CFR 820.75(b)(2)

21 CFR 820.198(e)

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Record Information

Company

Hospira, Inc.

Inspection Date

November 15, 2013

Product Type

Devices

Office

Atlanta District Office

People

ID: e87a2420-2ae9-450b-ba61-65d3dbff6f23

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