FDA Inspection 1031031 - Eli Lilly & Company - October 06, 2017

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Record Details

This FDA Inspection record concerns Eli Lilly & Company, with an inspection on October 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Eli Lilly & Company
Inspection Date: October 6, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 25d01567-d5de-4589-92b5-755e9eef7c48