Guangdong Kang Lai Light Ind Products Ltd
⚠️ Moderate Risk
FEI: 3003814534 • Guangzhou • CHINA
FEI Number
3003814534
Location
Guangzhou
Country
CHINAAddress
Long Dong Sha He, , Guangzhou, , China
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
CYCLAMATE
The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409
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.
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
Frequently Asked Questions
What is Guangdong Kang Lai Light Ind Products Ltd's FDA import refusal history?
Guangdong Kang Lai Light Ind Products Ltd (FEI: 3003814534) has 1 FDA import refusal record(s) in our database, spanning from 4/24/2003 to 4/24/2003.
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. Guangdong Kang Lai Light Ind Products Ltd's FEI number is 3003814534.
What types of violations has Guangdong Kang Lai Light Ind Products Ltd received?
Guangdong Kang Lai Light Ind Products Ltd 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 Guangdong Kang Lai Light Ind Products Ltd come from?
All FDA import refusal data for Guangdong Kang Lai Light Ind Products 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.