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FOUR M IMPORT AND EXPORT

⚠️ Moderate Risk

FEI: 3013030726 • Cairo, Al Qahirah • EGYPT

FEI

FEI Number

3013030726

📍

Location

Cairo, Al Qahirah

🇪🇬

Country

EGYPT
🏢

Address

11 Morkus Bechara Street, , Cairo, Al Qahirah, Egypt

Moderate Risk

FDA Import Risk Assessment

35.5
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

4
Total Refusals
4
Unique Violations
10/28/2016
Latest Refusal
7/31/2008
Earliest Refusal

Score Breakdown

Violation Severity
68.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
4.8×10%
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

2182×

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.

2491×

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.

621×

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).

831×

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

DateProductViolationsDivision
10/28/2016
12AFT10CHEESE, CREAM
218LIST INGRE
Division of Northeast Imports (DNEI)
10/28/2016
29BCT11SODA WATER WITH FRUIT FLAVOR, CARBONATED
218LIST INGRE
Division of Northeast Imports (DNEI)
10/20/2008
24AEE05FAVA BEAN
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
7/31/2008
21VYY14TAMARIND, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is FOUR M IMPORT AND EXPORT's FDA import refusal history?

FOUR M IMPORT AND EXPORT (FEI: 3013030726) has 4 FDA import refusal record(s) in our database, spanning from 7/31/2008 to 10/28/2016.

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. FOUR M IMPORT AND EXPORT's FEI number is 3013030726.

What types of violations has FOUR M IMPORT AND EXPORT received?

FOUR M IMPORT AND EXPORT has been cited for 4 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 FOUR M IMPORT AND EXPORT come from?

All FDA import refusal data for FOUR M IMPORT AND 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.