Imko Bv
✅ Low Risk
FEI: 3003631955 • Doetenchem • NETHERLANDS
FEI Number
3003631955
Location
Doetenchem
Country
NETHERLANDSAddress
29, , Doetenchem, , Netherlands
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/22/2002 | 23DMY07PEANUT, PASTE | 276PRESRV LBL | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Imko Bv's FDA import refusal history?
Imko Bv (FEI: 3003631955) has 1 FDA import refusal record(s) in our database, spanning from 4/22/2002 to 4/22/2002.
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. Imko Bv's FEI number is 3003631955.
What types of violations has Imko Bv received?
Imko Bv 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 Imko Bv come from?
All FDA import refusal data for Imko Bv 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.