483 RESPONSE
Eli Lilly & CompanyFDA 483_RESPONSE - Eli Lilly & Company - February 08, 2001
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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.
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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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