FDA Inspection
Eli Lilly & CompanyEli Lilly & Company – FDA Inspection, Jul 28, 2010
Record Details
This FDA Inspection record concerns Eli Lilly & Company, with an inspection on July 28, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Eli Lilly & Company
- Inspection Date
- July 28, 2010
- Product Type
- Drugs
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ID · af16178b-7509-4ae5-af8a-a06ca127ed63
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 675885
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.110(b)In-process materials specifications
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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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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