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Triple-M Products Co.,Ltd

⚠️ High Risk

FEI: 3017542569 • Bangkhuntien Bangkok, Bangkhuntien Bangkok • THAILAND

FEI

FEI Number

3017542569

📍

Location

Bangkhuntien Bangkok, Bangkhuntien Bangkok

🇹🇭

Country

THAILAND
🏢

Address

112/4 Soi Tientalay 24, Bangkhuntien-Chaytaley Rd. Thakham, Bangkhuntien Bangkok, Bangkhuntien Bangkok, Thailand

High Risk

FDA Import Risk Assessment

63.5
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
3/26/2025
Latest Refusal
3/26/2025
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
68.9×20%
Frequency
30.0×10%
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

2513×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

Refusal History

DateProductViolationsDivision
3/26/2025
24UGT29SEAWEED, DRIED OR PASTE
251POISONOUS
Division of West Coast Imports (DWCI)
3/26/2025
24UGT29SEAWEED, DRIED OR PASTE
251POISONOUS
Division of West Coast Imports (DWCI)
3/26/2025
24UGT29SEAWEED, DRIED OR PASTE
251POISONOUS
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Triple-M Products Co.,Ltd's FDA import refusal history?

Triple-M Products Co.,Ltd (FEI: 3017542569) has 3 FDA import refusal record(s) in our database, spanning from 3/26/2025 to 3/26/2025.

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. Triple-M Products Co.,Ltd's FEI number is 3017542569.

What types of violations has Triple-M Products Co.,Ltd received?

Triple-M Products Co.,Ltd 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 Triple-M Products Co.,Ltd come from?

All FDA import refusal data for Triple-M Products Co.,Ltd 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.