M & M & M PRODUCTS
⚠️ Moderate Risk
FEI: 3012609524 • Couva • TRINIDAD AND TOBAGO
FEI Number
3012609524
Location
Couva
Country
TRINIDAD AND TOBAGOAddress
72a Calcutta Road #1, M, , Couva, , Trinidad and Tobago
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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/29/2022 | 33EET06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 2/1/2018 | 21UGT05MANGO, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 62NEEDS FCE | Division of Northeast Imports (DNEI) |
| 6/28/2006 | 21TCY05MANGO, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is M & M & M PRODUCTS's FDA import refusal history?
M & M & M PRODUCTS (FEI: 3012609524) has 3 FDA import refusal record(s) in our database, spanning from 6/28/2006 to 9/29/2022.
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. M & M & M PRODUCTS's FEI number is 3012609524.
What types of violations has M & M & M PRODUCTS received?
M & M & M PRODUCTS 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 M & M & M PRODUCTS come from?
All FDA import refusal data for M & M & M PRODUCTS 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.