EL REY DE LA COSTA
⚠️ Moderate Risk
FEI: 2000012553 • Poza Rica, Veracruz • MEXICO
FEI Number
2000012553
Location
Poza Rica, Veracruz
Country
MEXICOAddress
Manuel Avila Camacho 2525, , Poza Rica, Veracruz, 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
Frequently Asked Questions
What is EL REY DE LA COSTA's FDA import refusal history?
EL REY DE LA COSTA (FEI: 2000012553) has 2 FDA import refusal record(s) in our database, spanning from 4/24/2007 to 4/24/2007.
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. EL REY DE LA COSTA's FEI number is 2000012553.
What types of violations has EL REY DE LA COSTA received?
EL REY DE LA COSTA 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 EL REY DE LA COSTA come from?
All FDA import refusal data for EL REY DE LA COSTA 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.