ARTURO GOMEZ FERNANDEZ
⚠️ Moderate Risk
FEI: 3014969280 • Puebla, Puebla • MEXICO
FEI Number
3014969280
Location
Puebla, Puebla
Country
MEXICOAddress
Calzada Del Conde Esquina Interior Norte, Central De Abastos Bodega 8, Puebla, Puebla, 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 |
|---|---|---|---|
| 1/3/2019 | 25JFC04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 1/3/2019 | 25JFC04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 12/18/2018 | 25JHC04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is ARTURO GOMEZ FERNANDEZ's FDA import refusal history?
ARTURO GOMEZ FERNANDEZ (FEI: 3014969280) has 3 FDA import refusal record(s) in our database, spanning from 12/18/2018 to 1/3/2019.
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. ARTURO GOMEZ FERNANDEZ's FEI number is 3014969280.
What types of violations has ARTURO GOMEZ FERNANDEZ received?
ARTURO GOMEZ FERNANDEZ 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 ARTURO GOMEZ FERNANDEZ come from?
All FDA import refusal data for ARTURO GOMEZ FERNANDEZ 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.