Profrutem S.A. De C.V.
⚠️ Moderate Risk
FEI: 3003924394 • Col. Los Pinos, Michoacan de Ocampo • MEXICO
FEI Number
3003924394
Location
Col. Los Pinos, Michoacan de Ocampo
Country
MEXICOAddress
Ebano 9, Zamora, Col. Los Pinos, Michoacan de Ocampo, 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
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/1/2003 | 37BHD25GUACAMOLE (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS) | 295LISTERIA | Southwest Import District Office (SWI-DO) |
| 7/1/2003 | 37BGD25GUACAMOLE (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS) | 295LISTERIA | Southwest Import District Office (SWI-DO) |
| 7/1/2003 | 37BGD25GUACAMOLE (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS) | 295LISTERIA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Profrutem S.A. De C.V.'s FDA import refusal history?
Profrutem S.A. De C.V. (FEI: 3003924394) has 3 FDA import refusal record(s) in our database, spanning from 7/1/2003 to 7/1/2003.
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. Profrutem S.A. De C.V.'s FEI number is 3003924394.
What types of violations has Profrutem S.A. De C.V. received?
Profrutem S.A. De C.V. 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 Profrutem S.A. De C.V. come from?
All FDA import refusal data for Profrutem S.A. De C.V. 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.