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

FDA Inspection 1082843 for Eli Lilly & Company on March 05, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1082843 for Eli Lilly & Company on March 05, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Eli Lilly & Company

Inspection Date

March 5, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

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

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