Van Rees Ceylon Limited
⚠️ Moderate Risk
FEI: 1000350912 • Peliyagoda, Gampaha • SRI LANKA
FEI Number
1000350912
Location
Peliyagoda, Gampaha
Country
SRI LANKAAddress
51/27 New Nuge Road, , Peliyagoda, Gampaha, Sri Lanka
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 Van Rees Ceylon Limited's FDA import refusal history?
Van Rees Ceylon Limited (FEI: 1000350912) has 2 FDA import refusal record(s) in our database, spanning from 6/5/2012 to 6/5/2012.
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. Van Rees Ceylon Limited's FEI number is 1000350912.
What types of violations has Van Rees Ceylon Limited received?
Van Rees Ceylon Limited 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 Van Rees Ceylon Limited come from?
All FDA import refusal data for Van Rees Ceylon Limited 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.