Laboratorios Undra, S.A. De C.V.
⚠️ Moderate Risk
FEI: 3003450804 • D.F. • MEXICO
FEI Number
3003450804
Location
D.F.
Country
MEXICOAddress
Calle Maiz # 255, Col. Xaltocan, Mexico, D.F., , Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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 |
|---|---|---|---|
| 9/30/2009 | 64ABR20TRICLOSAN (DISINFECTANT) | 75UNAPPROVED | Southwest Import District Office (SWI-DO) |
| 9/30/2009 | 64ABR20TRICLOSAN (DISINFECTANT) | 75UNAPPROVED | Southwest Import District Office (SWI-DO) |
| 11/27/2001 | 64ABR20TRICLOSAN (DISINFECTANT) | 75UNAPPROVED | Southwest Import District Office (SWI-DO) |
| 11/27/2001 | 64ABR20TRICLOSAN (DISINFECTANT) | 75UNAPPROVED | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Laboratorios Undra, S.A. De C.V.'s FDA import refusal history?
Laboratorios Undra, S.A. De C.V. (FEI: 3003450804) has 4 FDA import refusal record(s) in our database, spanning from 11/27/2001 to 9/30/2009.
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 Undra, S.A. De C.V.'s FEI number is 3003450804.
What types of violations has Laboratorios Undra, S.A. De C.V. received?
Laboratorios Undra, S.A. De C.V. 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 Undra, S.A. De C.V. come from?
All FDA import refusal data for Laboratorios Undra, S.A. De C.V. 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.