Kwan Shing Sea Products Co
⚠️ Moderate Risk
FEI: 3003581334 • Hong Kong • HONG KONG
FEI Number
3003581334
Location
Hong Kong
Country
HONG KONGAddress
142 Des Vouex Rd., , Hong Kong, , Hong Kong
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.
Refusal History
Frequently Asked Questions
What is Kwan Shing Sea Products Co's FDA import refusal history?
Kwan Shing Sea Products Co (FEI: 3003581334) has 2 FDA import refusal record(s) in our database, spanning from 1/7/2004 to 5/14/2004.
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. Kwan Shing Sea Products Co's FEI number is 3003581334.
What types of violations has Kwan Shing Sea Products Co received?
Kwan Shing Sea Products Co 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 Kwan Shing Sea Products Co come from?
All FDA import refusal data for Kwan Shing Sea Products Co 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.