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Keyie Co. Ltd

⚠️ Moderate Risk

FEI: 3004068629 • Trincity • TRINIDAD AND TOBAGO

FEI

FEI Number

3004068629

📍

Location

Trincity

🇹🇹
🏢

Address

29 Savannah Drive, , Trincity, , Trinidad and Tobago

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
6/21/2004
Latest Refusal
2/15/2004
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2412×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
6/21/2004
24FFC11CHINESE EGGPLANT, THAI EGGPLANT (FRUIT USED AS VEGETABLE)
241PESTICIDE
New York District Office (NYK-DO)
2/15/2004
24FFC11CHINESE EGGPLANT, THAI EGGPLANT (FRUIT USED AS VEGETABLE)
241PESTICIDE
New York District Office (NYK-DO)

Frequently Asked Questions

What is Keyie Co. Ltd's FDA import refusal history?

Keyie Co. Ltd (FEI: 3004068629) has 2 FDA import refusal record(s) in our database, spanning from 2/15/2004 to 6/21/2004.

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. Keyie Co. Ltd's FEI number is 3004068629.

What types of violations has Keyie Co. Ltd received?

Keyie 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 Keyie Co. Ltd come from?

All FDA import refusal data for Keyie 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.