Aurora Modulo 16-B
⚠️ Moderate Risk
FEI: 3011223774 • Jojutla, Morelos • MEXICO
FEI Number
3011223774
Location
Jojutla, Morelos
Country
MEXICOAddress
Carr Tequesquitengo Tlatenchi Mod 16-B, , Jojutla, Morelos, 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:
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
Refusal History
Frequently Asked Questions
What is Aurora Modulo 16-B's FDA import refusal history?
Aurora Modulo 16-B (FEI: 3011223774) has 1 FDA import refusal record(s) in our database, spanning from 12/20/2016 to 12/20/2016.
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. Aurora Modulo 16-B's FEI number is 3011223774.
What types of violations has Aurora Modulo 16-B received?
Aurora Modulo 16-B has been cited for 2 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 Aurora Modulo 16-B come from?
All FDA import refusal data for Aurora Modulo 16-B 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.