FDA Inspection 1037832 - Teleflex LLC - September 21, 2017

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Record Details

This FDA Inspection record concerns Teleflex LLC, with an inspection on September 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teleflex LLC
Inspection Date: September 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8783f278-4f54-4b26-9e51-cf6cfb41f8db