CFAI
C.F.A.I.
Government Data Intelligence Services

ELI LILLY & Co

Company
Found in 6 federal databases · 21 total records
chicago_biz 3 records
Chicago License: ELI LILLY & COMPANY
Limited Business License
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Chicago License: ELI LILLY & COMPANY
Limited Business License
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Chicago License: ELI LILLY & COMPANY
Limited Business License
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courtlistener_docket 5 records
Ousler, III v. ELI LILLY & COMPANY 2026-06-03
Federal docket 2:26-cv-03821 (paed); matched party 'ELI LILLY & COMPANY'
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Hafeli v. ELI LILLY & COMPANY 2026-05-13
Federal docket 2:26-cv-03254 (paed); matched party 'ELI LILLY & COMPANY'
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Moffett, III v. ELI LILLY & COMPANY 2026-05-01
Federal docket 2:26-cv-02885 (paed); matched party 'ELI LILLY & COMPANY'
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Henderson v. ELI LILLY & COMPANY 2026-04-15
Federal docket 2:26-cv-02463 (paed); matched party 'ELI LILLY & COMPANY'
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Cormier v. ELI LILLY & COMPANY 2026-04-01
Federal docket 2:26-cv-02124 (paed); matched party 'ELI LILLY & COMPANY'
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epa_echo 1 records
EPA ECHO: ELI LILLY 1992-10-13
Penalty assessed: $99,025. Type: Administrative - Formal
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fda 5 records
FDA Drug Recall: Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGUL 2024-04-24
Class II — CGMP Deviations
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FDA Drug Recall: Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per via 2021-10-20
Class I — SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.
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FDA Drug Recall: Trulicity (dulaglutide), 0.75 mg/0.5 mL, 4 Single-Dose Pens per box, Rx only, El 2021-09-01
Class II — Labeling: Label error on declared strength - autoinjector devices labeled as 0.75 mg / 0.5 mL actually contain 1.5 mg / 0.5 mL of product.
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FDA Drug Recall: Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx o 2021-08-18
Class II — cGMP deviations: Atypical appearance, decrease in size and change in color of the lyophilized cake of drug product.
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FDA Drug Recall: ERBITUX CETUXIMAB Injection, 200 mg/100 mL (2 mg/mL), 100 mL per single-use vial 2018-11-21
Class III — Labeling: Missing label; potential for missing primary container label on the vial.
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ftc_enforcement 1 records
Eli Lilly & Co. and Sepracor, Inc. 2003-06-27
FTC live enforcement action FY2003; matched respondent 'Eli Lilly & Co.'
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lobbying 4 records
Lobbying Client: ELI LILLY & COMPANY
Lobbied by THE HARPLE GROUP, LLC — Biopharmaceutical company
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Lobbying Client: ELI LILLY & COMPANY
Lobbied by DLA PIPER LLP (US) — Biopharmaceutical company
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Lobbying Client: ELI LILLY & COMPANY
Lobbied by THE HARPLE GROUP, LLC — Biopharmaceutical company
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Lobbying Client: ELI LILLY & COMPANY
Lobbied by DLA PIPER LLP (US) — Biopharmaceutical company
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OSHA 1 records
OSHA Inspection (Planned) - Eli Lilly & Co 1983-04-28
OSHA inspection at Eli Lilly & Co, Roanoke, VA. NAICS: 000000. SIC: 3089
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SEC EDGAR 1 records
SEC Registered: ELI LILLY & Co (LLY)
Ticker: LLY | CIK: 59478
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