FDA Inspection 584062 - Hospira, Inc. - April 29, 2009

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Record Details

This FDA Inspection record concerns Hospira, Inc., with an inspection on April 29, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Hospira, Inc.
Inspection Date: April 29, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6a04f3be-71a3-4a89-b2c3-ffe66fb64e03

Violation Codes10

21 CFR 211.110(a)21 CFR 211.113(b)21 CFR 211.160(b)21 CFR 211.180(e)(1)21 CFR 211.180(e)(2)21 CFR 211.186(b)(9)21 CFR 211.19221 CFR 211.22(d)21 CFR 211.46(c)21 CFR 211.68(b)

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