FDA Inspection 1041855 - Stericycle Inc - February 21, 2018

FDA Inspection 1041855 for Stericycle Inc on February 21, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1041855 for Stericycle Inc on February 21, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.198(a)

21 CFR 820.20(c)

21 CFR 820.22

21 CFR 820.50

21 CFR 820.80(a)

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Record Information

Company

Stericycle Inc

Inspection Date

February 21, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f861188e-c22e-418f-b0ef-e26d60771fdd

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