Rainbow International B.V.
⚠️ Moderate Risk
FEI: 3004039301 • De Lier, Zuid-Holland • NETHERLANDS
FEI Number
3004039301
Location
De Lier, Zuid-Holland
Country
NETHERLANDSAddress
Poortcamp 9, , De Lier, Zuid-Holland, Netherlands
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
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 |
|---|---|---|---|
| 12/3/2004 | 24FFC07PEPPER, SWEET (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 6/14/2004 | 24FHC07PEPPER, SWEET (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Detroit District Office (DET-DO) |
| 5/13/2004 | 24FFC07PEPPER, SWEET (FRUIT USED AS VEGETABLE) | 241PESTICIDE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Rainbow International B.V.'s FDA import refusal history?
Rainbow International B.V. (FEI: 3004039301) has 3 FDA import refusal record(s) in our database, spanning from 5/13/2004 to 12/3/2004.
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. Rainbow International B.V.'s FEI number is 3004039301.
What types of violations has Rainbow International B.V. received?
Rainbow International B.V. 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 Rainbow International B.V. come from?
All FDA import refusal data for Rainbow International B.V. 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.