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Zein Atat

⚠️ Moderate Risk

FEI: 3007366656 • Beirut • LEBANON

FEI

FEI Number

3007366656

📍

Location

Beirut

🇱🇧

Country

LEBANON
🏢

Address

Unknown Street, , Beirut, , Lebanon

Moderate Risk

FDA Import Risk Assessment

38.7
LowModerateHighCritical

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

Statistics

9
Total Refusals
9
Unique Violations
1/6/2011
Latest Refusal
1/6/2011
Earliest Refusal

Score Breakdown

Violation Severity
46.5×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

4714×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

3202×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3242×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

752×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4822×

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.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

2181×

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.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
1/6/2011
54YBA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
11UNSAFE COL
320LACKS FIRM
New Orleans District Office (NOL-DO)
1/6/2011
54YBL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
482NUTRIT LBL
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/6/2011
53RD05HAIR PREPARATIONS (NON-COLORING), COSMETIC PRODUCTS CONTAINING ANIMAL BY-PRODUCTS (BOVINE)
475COSMETLBLG
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/6/2011
53FH01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI
471CSTIC LBLG
473LABELING
New Orleans District Office (NOL-DO)
1/6/2011
53RD05HAIR PREPARATIONS (NON-COLORING), COSMETIC PRODUCTS CONTAINING ANIMAL BY-PRODUCTS (BOVINE)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
1/6/2011
53RD05HAIR PREPARATIONS (NON-COLORING), COSMETIC PRODUCTS CONTAINING ANIMAL BY-PRODUCTS (BOVINE)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
1/6/2011
53RD05HAIR PREPARATIONS (NON-COLORING), COSMETIC PRODUCTS CONTAINING ANIMAL BY-PRODUCTS (BOVINE)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
1/6/2011
54YBA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
New Orleans District Office (NOL-DO)
1/6/2011
54YBA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
320LACKS FIRM
324NO ENGLISH
473LABELING
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Zein Atat's FDA import refusal history?

Zein Atat (FEI: 3007366656) has 9 FDA import refusal record(s) in our database, spanning from 1/6/2011 to 1/6/2011.

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. Zein Atat's FEI number is 3007366656.

What types of violations has Zein Atat received?

Zein Atat has been cited for 9 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 Zein Atat come from?

All FDA import refusal data for Zein Atat 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.