FDA Inspection 972671 - George Tiemann & Co. - June 01, 2016

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Record Details

This FDA Inspection record concerns George Tiemann & Co., with an inspection on June 1, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: George Tiemann & Co.
Inspection Date: June 1, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 15599f71-5b1a-4516-bf58-231a59de962b

Violation Codes1

21 CFR 820.20(e)

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