Eli Lilly & Company – FDA Warning Letter Response, Feb 23, 2001

Record Details

This WARNING LETTER RESPONSE record concerns Eli Lilly & Company, with an inspection on February 23, 2001, issued by the Center for Devices and Radiological Health, covering devices.

Company: Eli Lilly & Company
Inspection date: February 23, 2001
Product type: Devices
Office: Center for Devices and Radiological Health
People: Thomas J. (Regulatory Counsel)
Judith A. Putz (Ms.)
Hung V. Le (Investigator)
Patricia Cochran
Jeffrey Sommers

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ID · e90881d9-e2fa-473e-ab9d-4415ee00f701

Violation Codes9

21 CFR 21021 CFR 211.2221 CFR 211.10021 CFR 211.113(b)21 CFR 211.16021 CFR 211.42(c)(5)21 CFR 211.42(b)21 CFR 211.6821 U.S.C. 501(a)(2)(B)

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WARNING LETTER RESPONSE

Eli Lilly & CompanyFebruary 23, 2001

Eli Lilly & Company – FDA Warning Letter Response, Feb 23, 2001

Record Details

This WARNING LETTER RESPONSE record concerns Eli Lilly & Company, with an inspection on February 23, 2001, issued by the Center for Devices and Radiological Health, covering devices.

Company: Eli Lilly & Company
Inspection date: February 23, 2001
Product type: Devices
Office: Center for Devices and Radiological Health
People: Thomas J. (Regulatory Counsel)
Judith A. Putz (Ms.)
Hung V. Le (Investigator)
Patricia Cochran
Jeffrey Sommers

View Company Profile

ID · e90881d9-e2fa-473e-ab9d-4415ee00f701

Violation Codes9

21 CFR 21021 CFR 211.2221 CFR 211.10021 CFR 211.113(b)21 CFR 211.16021 CFR 211.42(c)(5)21 CFR 211.42(b)21 CFR 211.6821 U.S.C. 501(a)(2)(B)

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.

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Explore Eli Lilly & Company