FDA Inspection 942202 - Hospira, Inc. - September 24, 2015

FDA Inspection 942202 for Hospira, Inc. on September 24, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 942202 for Hospira, Inc. on September 24, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Hospira, Inc.

Inspection Date

September 24, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 5ffad654-432c-4279-bb5b-e6ff8854b145

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