FDA Inspection 633739 - Covidien LP - December 10, 2009

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Record Details

This FDA Inspection record concerns Covidien LP, with an inspection on December 10, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Covidien LP
Inspection Date: December 10, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8c49450f-c5f4-465c-a536-5572703cc4f7

Violation Codes1

21 CFR 803.17(a)(1)

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