Van Der Velden
⚠️ High Risk
FEI: 3010237374 • Liessl • NETHERLANDS
FEI Number
3010237374
Location
Liessl
Country
NETHERLANDSAddress
Eikenlorn 33, , Liessl, , Netherlands
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/18/2015 | 25JGB03LEEK (A TYPE OF ONION) (ROOT & TUBER VEGETABLE) | 241PESTICIDE | New England District Office (NWE-DO) |
| 1/15/2015 | 25JGC03LEEK (A TYPE OF ONION) (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Baltimore District Office (BLT-DO) |
| 9/19/2014 | 25JGC03LEEK (A TYPE OF ONION) (ROOT & TUBER VEGETABLE) | 241PESTICIDE | New York District Office (NYK-DO) |
| 9/16/2014 | 25JGC03LEEK (A TYPE OF ONION) (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Van Der Velden's FDA import refusal history?
Van Der Velden (FEI: 3010237374) has 4 FDA import refusal record(s) in our database, spanning from 9/16/2014 to 6/18/2015.
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 Der Velden's FEI number is 3010237374.
What types of violations has Van Der Velden received?
Van Der Velden 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 Der Velden come from?
All FDA import refusal data for Van Der Velden 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.