FDA Inspection 609930 - Teleflex Medical, Inc. - August 27, 2009

Record Details

This FDA Inspection record concerns Teleflex Medical, Inc., with an inspection on August 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teleflex Medical, Inc.
Inspection Date: August 27, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1c057bdf-c88f-495b-8f86-3bbc43c38e9a

Violation Codes2

21 CFR 820.100(a)21 CFR 820.100(a)(2)

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