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YUEN TAT TRADING COMPANY

⚠️ Moderate Risk

FEI: 3009862834 • Mong Kok, Kowloon • HONG KONG

FEI

FEI Number

3009862834

📍

Location

Mong Kok, Kowloon

🇭🇰

Country

HONG KONG
🏢

Address

Rt/F, C/Flat, Mo Kwan House; 438-440 Portland Street, Mong Kok, Kowloon, Hong Kong

Moderate Risk

FDA Import Risk Assessment

46.4
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

6
Total Refusals
4
Unique Violations
4/13/2012
Latest Refusal
7/27/2010
Earliest Refusal

Score Breakdown

Violation Severity
83.8×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
35.0×10%
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

2495×

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.

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

29201×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
4/13/2012
20QGH05CORE FRUIT, DRIED OR PASTE (PRICKLE PEAR CACTUS)
249FILTHY
New York District Office (NYK-DO)
2/8/2012
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
New York District Office (NYK-DO)
2/8/2012
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
New York District Office (NYK-DO)
2/8/2012
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
New York District Office (NYK-DO)
5/31/2011
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2920PESTICIDES
New York District Office (NYK-DO)
7/27/2010
54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
249FILTHY
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is YUEN TAT TRADING COMPANY's FDA import refusal history?

YUEN TAT TRADING COMPANY (FEI: 3009862834) has 6 FDA import refusal record(s) in our database, spanning from 7/27/2010 to 4/13/2012.

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. YUEN TAT TRADING COMPANY's FEI number is 3009862834.

What types of violations has YUEN TAT TRADING COMPANY received?

YUEN TAT TRADING COMPANY has been cited for 4 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 YUEN TAT TRADING COMPANY come from?

All FDA import refusal data for YUEN TAT TRADING COMPANY 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.