FDA Inspection 1031233 - Hospira, Inc., A Pfizer Company - October 27, 2017

FDA Inspection 1031233 for Hospira, Inc., A Pfizer Company on October 27, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1031233 for Hospira, Inc., A Pfizer Company on October 27, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Hospira, Inc., A Pfizer Company

Inspection Date

October 27, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: b47e08bd-8a1b-4f71-a6fb-000cc18f9dd3

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