FDA Inspection 962757 - Teleflex LLC (NADC 2) - March 03, 2016

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Record Details

This FDA Inspection record concerns Teleflex LLC (NADC 2), with an inspection on March 3, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teleflex LLC (NADC 2)
Inspection Date: March 3, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b8c4c4a0-04a9-4609-ad90-d6f80152c188