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FADI AMER SBEIHAT

⚠️ Moderate Risk

FEI: 3030255032 • Jerusalem • ISRAEL

FEI

FEI Number

3030255032

📍

Location

Jerusalem

🇮🇱

Country

ISRAEL
🏢

Address

5, Hafez I'Brahim, , Jerusalem, , Israel

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
3/4/2024
Latest Refusal
3/4/2024
Earliest Refusal

Score Breakdown

Violation Severity
41.5×40%
Refusal Volume
31.3×30%
Recency
48.5×20%
Frequency
60.0×10%
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

3246×

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)).

4825×

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.

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
3/4/2024
12CYY99CHEESE PRODUCTS, NON-STANDARDIZED, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/4/2024
12YYY99CHEESE AND CHEESE PRODUCTS, NOT ELSEWHERE MENTIONED, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/4/2024
33EYY07JELLIED CANDIES, HARD (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/4/2024
33BYY01CARAMEL CANDY BAR, HARD, WITH COCONUT (WITHOUT CHOCOLATE)
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/4/2024
33BYY01CARAMEL CANDY BAR, HARD, WITH COCONUT (WITHOUT CHOCOLATE)
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/4/2024
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is FADI AMER SBEIHAT's FDA import refusal history?

FADI AMER SBEIHAT (FEI: 3030255032) has 6 FDA import refusal record(s) in our database, spanning from 3/4/2024 to 3/4/2024.

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. FADI AMER SBEIHAT's FEI number is 3030255032.

What types of violations has FADI AMER SBEIHAT received?

FADI AMER SBEIHAT 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 FADI AMER SBEIHAT come from?

All FDA import refusal data for FADI AMER SBEIHAT 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.