FDA 483_RESPONSE - Eli Lilly & Company - February 08, 2001

Record Details

This 483 RESPONSE record concerns Eli Lilly & Company, with an inspection on February 8, 2001, issued by the Center for Devices and Radiological Health, covering devices.

Company: Eli Lilly & Company
Inspection Date: February 8, 2001
Product Type: Devices
Office: Center for Devices and Radiological Health
People: Raymond Mlecko (Mr.)
Steven E. Porter (Program Division Director)

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ID · 662d6e8c-e3c8-464f-befc-6266f2c566db

Violation Codes2

FD&C Act 801(a)(3)21 CFR 210

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