Guillermo Padilla Gonzalez
⚠️ Moderate Risk
FEI: 3006199739 • Col. Lazaro Cardenas Sur, Puebla • MEXICO
FEI Number
3006199739
Location
Col. Lazaro Cardenas Sur, Puebla
Country
MEXICOAddress
Calle Aldama Sur No. 403, Tehuacan, Col. Lazaro Cardenas Sur, 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 |
|---|---|---|---|
| 5/6/2013 | 24TFC99LEAF & STEM VEGETABLES, N.E.C. | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 5/6/2013 | 20NJC06PRICKLE PEAR CACTUS - EDIBLE STEMS OR PADS (CORE FRUIT) (CORE FRUIT) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 11/7/2011 | 20NJC06PRICKLE PEAR CACTUS - EDIBLE STEMS OR PADS (CORE FRUIT) (CORE FRUIT) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Guillermo Padilla Gonzalez's FDA import refusal history?
Guillermo Padilla Gonzalez (FEI: 3006199739) has 3 FDA import refusal record(s) in our database, spanning from 11/7/2011 to 5/6/2013.
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. Guillermo Padilla Gonzalez's FEI number is 3006199739.
What types of violations has Guillermo Padilla Gonzalez received?
Guillermo Padilla Gonzalez 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 Guillermo Padilla Gonzalez come from?
All FDA import refusal data for Guillermo Padilla Gonzalez 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.