Laboratorios Diba, S.A.
⚠️ High Risk
FEI: 3004534358 • Guadalajara, Jalisco • MEXICO
FEI Number
3004534358
Location
Guadalajara, Jalisco
Country
MEXICOAddress
Calle Escorza # 728, Col. MODERNA, Guadalajara, Jalisco, Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/1/2025 | 54YGY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 10/12/2017 | 66VDY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 9/14/2017 | 64GCB29LEVONORGESTREL (ESTROGEN) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 8/13/2012 | 64GDY29LEVONORGESTREL (ESTROGEN) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 8/5/2011 | 62ODB14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 1/15/2008 | 65QCA22METHOCARBAMOL (RELAXANT) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 3/29/2005 | 64LCA60TRIAMCINOLONE (GLUCOCORTICOID) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Laboratorios Diba, S.A.'s FDA import refusal history?
Laboratorios Diba, S.A. (FEI: 3004534358) has 7 FDA import refusal record(s) in our database, spanning from 3/29/2005 to 12/1/2025.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Laboratorios Diba, S.A.'s FEI number is 3004534358.
What types of violations has Laboratorios Diba, S.A. received?
Laboratorios Diba, S.A. has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Laboratorios Diba, S.A. come from?
All FDA import refusal data for Laboratorios Diba, S.A. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.