Egyption Company
✅ Low Risk
FEI: 3009660313 • Al Qahira, Al Qahira • EGYPT
FEI Number
3009660313
Location
Al Qahira, Al Qahira
Country
EGYPTAddress
32 El Ahram Street, , Al Qahira, Al Qahira, Egypt
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
Refusal History
Frequently Asked Questions
What is Egyption Company's FDA import refusal history?
Egyption Company (FEI: 3009660313) has 1 FDA import refusal record(s) in our database, spanning from 11/30/2015 to 11/30/2015.
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. Egyption Company's FEI number is 3009660313.
What types of violations has Egyption Company received?
Egyption Company has been cited for 2 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 Egyption Company come from?
All FDA import refusal data for Egyption Company 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.