FDA Inspection 897366 - TELEFLEX LLC - August 22, 2014

FDA Inspection 897366 for TELEFLEX LLC on August 22, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 897366 for TELEFLEX LLC on August 22, 2014. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(b)

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Record Information

Company

TELEFLEX LLC

Inspection Date

August 22, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb510fc5-2b34-4205-b375-320bf8c1ee94

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