FDA Inspection 1022942 - E.A. Beck & Co. - August 10, 2017

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Record Details

This FDA Inspection record concerns E.A. Beck & Co., with an inspection on August 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: E.A. Beck & Co.
Inspection Date: August 10, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 01baa9a6-631b-4a51-b2c3-ff8007ee7913