Al Izze Co
✅ Low Risk
FEI: 3006316341 • Amman, The Capital • JORDAN
FEI Number
3006316341
Location
Amman, The Capital
Country
JORDANAddress
Al Youbil Circle, , Amman, The Capital, Jordan
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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/5/2007 | 64MDY99GONAD-STIMULATING PRINCIPLE N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Al Izze Co's FDA import refusal history?
Al Izze Co (FEI: 3006316341) has 1 FDA import refusal record(s) in our database, spanning from 7/5/2007 to 7/5/2007.
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. Al Izze Co's FEI number is 3006316341.
What types of violations has Al Izze Co received?
Al Izze Co 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 Al Izze Co come from?
All FDA import refusal data for Al Izze Co 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.