Ezt Mohamed Kobeisy
⚠️ Moderate Risk
FEI: 3012785850 • Kalyobiah, EG-KB • EGYPT
FEI Number
3012785850
Location
Kalyobiah, EG-KB
Country
EGYPTAddress
Aboelgheait. Road, , Kalyobiah, EG-KB, Egypt
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
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
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.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/9/2017 | 24BGT26LUPIN BEAN, DRIED OR PASTE | Division of Northeast Imports (DNEI) | |
| 3/9/2017 | 24BGT26LUPIN BEAN, DRIED OR PASTE | Division of Northeast Imports (DNEI) | |
| 3/9/2017 | 25JCT25ONION BULB (YELLOW, WHITE, RED, ETC.) (ROOT & TUBER VEGETABLE) | Division of Northeast Imports (DNEI) | |
| 3/9/2017 | 20GCT04LEMON (CITRUS) | Division of Northeast Imports (DNEI) | |
| 3/9/2017 | 24FCT08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Ezt Mohamed Kobeisy's FDA import refusal history?
Ezt Mohamed Kobeisy (FEI: 3012785850) has 5 FDA import refusal record(s) in our database, spanning from 3/9/2017 to 3/9/2017.
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. Ezt Mohamed Kobeisy's FEI number is 3012785850.
What types of violations has Ezt Mohamed Kobeisy received?
Ezt Mohamed Kobeisy has been cited for 7 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 Ezt Mohamed Kobeisy come from?
All FDA import refusal data for Ezt Mohamed Kobeisy 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.