FDA Inspection
Eli Lilly & CompanyEli Lilly & Company – FDA Inspection, Dec 6, 2013
Record Details
This FDA Inspection record concerns Eli Lilly & Company, with an inspection on December 6, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Eli Lilly & Company
- Inspection Date
- December 6, 2013
- Product Type
- Devices
View Company Profile
ID · 7409bf6c-161f-4b59-92d4-2998771aa7af
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 858117
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Eli Lilly & Company
35| Date | Classification | Office | Project area |
|---|---|---|---|
| January 9, 2026 | NAI | Bioresearch Monitoring | |
| May 20, 2025 | VAI | Detroit District Office | Drug Quality Assurance |
| March 27, 2025 | Not classified | Detroit District Office | |
| January 15, 2025 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| October 6, 2023 | Not classified | Detroit District Office |
Other documents for Eli Lilly & Company
- FDA Inspection 1298628 - 2026-01-09
- FDA Inspection 1270621 - 2025-05-20
- FDA Inspection 1260339 - 2025-03-27
- FDA Inspection 1229895 - 2025-01-15
- FDA Inspection 1220489 - 2023-10-06
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