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Kasih Canned Food Production

⚠️ Moderate Risk

FEI: 3001322136 • Amman, The Capital • JORDAN

FEI

FEI Number

3001322136

📍

Location

Amman, The Capital

🇯🇴

Country

JORDAN
🏢

Address

Otbah As-Sulaymi Street, Building 7 #, , Amman, The Capital, Jordan

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

6
Total Refusals
8
Unique Violations
2/15/2023
Latest Refusal
12/5/2001
Earliest Refusal

Score Breakdown

Violation Severity
63.1×40%
Refusal Volume
31.3×30%
Recency
41.9×20%
Frequency
2.8×10%
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

835×

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.

622×

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).

3241×

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)).

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.

3201×

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.

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.

38411×

AF-NONRSP

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to have been prepared or packed under insanitary conditions whereby it may have been rendered injurious to health due to inadequate processing in that the scheduled process filed by the manufacturer for this acidified food pursuant to 21 CFR 108.25 (c)(2) appears to be inadequate to protect the public health.

3211×

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.

Refusal History

DateProductViolationsDivision
2/15/2023
37BFT26HOMMUS, HUMMUS (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS)
3841AF-NONRSP
83NO PROCESS
Division of Southeast Imports (DSEI)
6/8/2018
09FFE32MILK PROTEIN CONCENTRATE, GOAT MILK
324NO ENGLISH
328USUAL NAME
62NEEDS FCE
83NO PROCESS
Division of Southwest Imports (DSWI)
9/7/2007
17HVF66SHEEP, PRODUCTS N.E.C.
83NO PROCESS
Florida District Office (FLA-DO)
3/24/2004
09GEE15YOGURT (PLAIN, FLAVORED OR FRUIT ADDED), SHEEP MILK
83NO PROCESS
Baltimore District Office (BLT-DO)
7/29/2003
38AHF99SOUP, N.E.C.
62NEEDS FCE
83NO PROCESS
Chicago District Office (CHI-DO)
12/5/2001
24HFE50TOMATO, DRIED
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Kasih Canned Food Production's FDA import refusal history?

Kasih Canned Food Production (FEI: 3001322136) has 6 FDA import refusal record(s) in our database, spanning from 12/5/2001 to 2/15/2023.

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. Kasih Canned Food Production's FEI number is 3001322136.

What types of violations has Kasih Canned Food Production received?

Kasih Canned Food Production has been cited for 8 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 Kasih Canned Food Production come from?

All FDA import refusal data for Kasih Canned Food Production 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.