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Mounir Bissat Factories

⚠️ Moderate Risk

FEI: 3004307194 • Saida • LEBANON

FEI

FEI Number

3004307194

📍

Location

Saida

🇱🇧

Country

LEBANON
🏢

Address

Ghazieh, Industrial Zone II, Bissat Bld., , Saida, , Lebanon

Moderate Risk

FDA Import Risk Assessment

30.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
4/19/2021
Latest Refusal
10/28/2009
Earliest Refusal

Score Breakdown

Violation Severity
58.6×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
2.6×10%
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.

92×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

33201×

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)].

4821×

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

DateProductViolationsDivision
4/19/2021
33LGT99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
218LIST INGRE
9SALMONELLA
Division of Northeast Imports (DNEI)
4/19/2021
33LGT99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
9SALMONELLA
Division of Northeast Imports (DNEI)
10/28/2009
33GHT99SOFT CANDY WITH NUTS OR NUT PRODUCTS, N.E.C. (WITHOUT CHOCOLATE)
218LIST INGRE
328USUAL NAME
3320TRANSFAT
482NUTRIT LBL
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Mounir Bissat Factories's FDA import refusal history?

Mounir Bissat Factories (FEI: 3004307194) has 3 FDA import refusal record(s) in our database, spanning from 10/28/2009 to 4/19/2021.

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. Mounir Bissat Factories's FEI number is 3004307194.

What types of violations has Mounir Bissat Factories received?

Mounir Bissat Factories has been cited for 5 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 Mounir Bissat Factories come from?

All FDA import refusal data for Mounir Bissat Factories 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.