FDA Inspection 858921 - Teleflex Medical Tuttlingen GmbH - November 05, 2013

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Record Details

This FDA Inspection record concerns Teleflex Medical Tuttlingen GmbH, with an inspection on November 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teleflex Medical Tuttlingen GmbH
Inspection Date: November 5, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 740a7480-98cc-4289-95ca-ec837f50cdb4

Violation Codes2

21 CFR 820.100(b)21 CFR 820.50(a)

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