Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1819470.
Observations3
Issue DateJune 16, 2023
StatusNo Warning Letter
Establishment TypePharmaceutical and Medical Device Manufacturer
Related Inspections10
Establishment Details
Firm
Eli Lilly & Company
Location
Indianapolis, Indiana, United States
FEI Number
1819470
Establishment Type
Pharmaceutical and Medical Device Manufacturer
Product Type
Drugs
Issue Date
June 16, 2023
Country
United States
Inspection History, 2020 to 2026
NAI5
VAI5
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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