Luis Alfredo Mercado Herrera
⚠️ Moderate Risk
FEI: 3004523687 • Tecoman, Colima • MEXICO
FEI Number
3004523687
Location
Tecoman, Colima
Country
MEXICOAddress
Avenida Insurgentes # 1369, Col. Griselda Alvarez, Tecoman, Tecoman, Colima, 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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/8/2010 | 24AFC99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 10/8/2010 | 24AFC99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 9/19/2006 | 25JGC04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Luis Alfredo Mercado Herrera's FDA import refusal history?
Luis Alfredo Mercado Herrera (FEI: 3004523687) has 3 FDA import refusal record(s) in our database, spanning from 9/19/2006 to 11/8/2010.
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. Luis Alfredo Mercado Herrera's FEI number is 3004523687.
What types of violations has Luis Alfredo Mercado Herrera received?
Luis Alfredo Mercado Herrera 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 Luis Alfredo Mercado Herrera come from?
All FDA import refusal data for Luis Alfredo Mercado Herrera 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.