Emko Products Ltd
⚠️ Moderate Risk
FEI: 3003590971 • London • UNITED KINGDOM
FEI Number
3003590971
Location
London
Country
UNITED KINGDOMAddress
The Ridge Hendon Wood La, , London, , United Kingdom
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
LACK NOTIF
Adulterated, 801(a)(3), lack of documentation establishing that the infant formula meets all notification conditions required by 412(c) or 412(d), Prohibited Act, Section 301(s).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/25/2002 | 40CEE01MILK BASE FORMULA PRODUCT (BABY) | 2160LACK NOTIF | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Emko Products Ltd's FDA import refusal history?
Emko Products Ltd (FEI: 3003590971) has 1 FDA import refusal record(s) in our database, spanning from 3/25/2002 to 3/25/2002.
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. Emko Products Ltd's FEI number is 3003590971.
What types of violations has Emko Products Ltd received?
Emko Products Ltd 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 Emko Products Ltd come from?
All FDA import refusal data for Emko Products Ltd 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.