KEYIE CO. LTD. (Facility #1)
⚠️ Moderate Risk
FEI: 3010145914 • Valencia • TRINIDAD AND TOBAGO
FEI Number
3010145914
Location
Valencia
Country
TRINIDAD AND TOBAGOAddress
43 VALENCIA OLD ROAD VAT# 119311, , Valencia, , 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.
LACKS N/C
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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
Refusal History
Frequently Asked Questions
What is KEYIE CO. LTD. (Facility #1)'s FDA import refusal history?
KEYIE CO. LTD. (Facility #1) (FEI: 3010145914) has 1 FDA import refusal record(s) in our database, spanning from 3/1/2016 to 3/1/2016.
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. (Facility #1)'s FEI number is 3010145914.
What types of violations has KEYIE CO. LTD. (Facility #1) received?
KEYIE CO. LTD. (Facility #1) has been cited for 3 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. (Facility #1) come from?
All FDA import refusal data for KEYIE CO. LTD. (Facility #1) 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.