FDA Inspection 890794 - Welch Allyn Inc - August 13, 2014

FDA Inspection 890794 for Welch Allyn Inc on August 13, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 890794 for Welch Allyn Inc on August 13, 2014. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.198(a)

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Record Information

Company

Welch Allyn Inc

Inspection Date

August 13, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe33d6a7-462d-4da5-8ca2-65058fc5ace9

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