Guzguz Tessema General Export
⚠️ Moderate Risk
FEI: 3003617681 • Addis Ababa • ETHIOPIA
FEI Number
3003617681
Location
Addis Ababa
Country
ETHIOPIAAddress
P O Box 6740, , Addis Ababa, , Ethiopia
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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
Frequently Asked Questions
What is Guzguz Tessema General Export's FDA import refusal history?
Guzguz Tessema General Export (FEI: 3003617681) has 2 FDA import refusal record(s) in our database, spanning from 6/7/2002 to 6/7/2002.
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. Guzguz Tessema General Export's FEI number is 3003617681.
What types of violations has Guzguz Tessema General Export received?
Guzguz Tessema General Export 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 Guzguz Tessema General Export come from?
All FDA import refusal data for Guzguz Tessema General Export 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.