FDA Inspection 930829 - Teleflex Medical Europe Ltd - June 05, 2015

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Record Details

This FDA Inspection record concerns Teleflex Medical Europe Ltd, with an inspection on June 5, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teleflex Medical Europe Ltd
Inspection Date: June 5, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b33c44fa-7a2c-4861-9388-c169e3283c67