MANUEL AZCONA ZENTENO
⚠️ Moderate Risk
FEI: 3004315508 • San Andres Cholula, Puebla • MEXICO
FEI Number
3004315508
Location
San Andres Cholula, Puebla
Country
MEXICOAddress
20 De Noviembre No 32, Colonia Emiliano Zapata, San Andres Cholula, 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
Frequently Asked Questions
What is MANUEL AZCONA ZENTENO's FDA import refusal history?
MANUEL AZCONA ZENTENO (FEI: 3004315508) has 2 FDA import refusal record(s) in our database, spanning from 2/6/2004 to 10/21/2005.
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. MANUEL AZCONA ZENTENO's FEI number is 3004315508.
What types of violations has MANUEL AZCONA ZENTENO received?
MANUEL AZCONA ZENTENO 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 MANUEL AZCONA ZENTENO come from?
All FDA import refusal data for MANUEL AZCONA ZENTENO 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.