Eli Lilly & Company – FDA 483 Response, Feb 8, 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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483 RESPONSE

Eli Lilly & CompanyFebruary 8, 2001

Eli Lilly & Company – FDA 483 Response, Feb 8, 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)

View Company Profile

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

Violation Codes2

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

Full citation text and observation details available on the Dashboard.

One record shows the event. A profile shows the pattern.

Buy this document for the source file and details behind this single event.

Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.

Explore Eli Lilly & Company