Guillermo Mendez
⚠️ Moderate Risk
FEI: 3003978819 • Santiago • DOMINICAN REPUBLIC
FEI Number
3003978819
Location
Santiago
Country
DOMINICAN REPUBLICAddress
Calle B Esq.C Urbanizacion Noreda, , Santiago, , Dominican Republic
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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/2/2012 | 12AWS12CHEESE, EDAM | New York District Office (NYK-DO) | |
| 5/2/2012 | 12AWS05CHEESE, CHEDDAR | New York District Office (NYK-DO) | |
| 7/7/2011 | 12AWS05CHEESE, CHEDDAR | New York District Office (NYK-DO) | |
| 5/31/2006 | 12AWS05CHEESE, CHEDDAR | 308MFR INSAN | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Guillermo Mendez's FDA import refusal history?
Guillermo Mendez (FEI: 3003978819) has 4 FDA import refusal record(s) in our database, spanning from 5/31/2006 to 5/2/2012.
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 Mendez's FEI number is 3003978819.
What types of violations has Guillermo Mendez received?
Guillermo Mendez 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 Guillermo Mendez come from?
All FDA import refusal data for Guillermo Mendez 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.