FDA Inspection 1082843 - Eli Lilly & Company - March 05, 2019

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Record Details

This FDA Inspection record concerns Eli Lilly & Company, with an inspection on March 5, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Eli Lilly & Company
Inspection Date: March 5, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · fa387f59-3695-40c6-ba7f-8a4a486ca920