FDA Inspection 1025854 - Teleflex Medical, Inc. - September 20, 2017

Record Details

This FDA Inspection record concerns Teleflex Medical, Inc., with an inspection on September 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teleflex Medical, Inc.
Inspection Date: September 20, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dd0fc511-d6d3-43d5-9d87-ea8cd8dc0395