FDA Inspection 698018 - Teleflex Medical Europe Ltd - November 04, 2010

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Record Details

This FDA Inspection record concerns Teleflex Medical Europe Ltd, with an inspection on November 4, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teleflex Medical Europe Ltd
Inspection Date: November 4, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 7cc07782-01b8-4920-9bbf-fa4e08ef6151