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Shezan International Limited

⚠️ High Risk

FEI: 3010122553 • Karachi, Sindh • PAKISTAN

FEI

FEI Number

3010122553

📍

Location

Karachi, Sindh

🇵🇰

Country

PAKISTAN
🏢

Address

No. 22-Plot L-9, Block, , Karachi, Sindh, Pakistan

High Risk

FDA Import Risk Assessment

60.1
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

16
Total Refusals
9
Unique Violations
5/30/2025
Latest Refusal
5/15/2002
Earliest Refusal

Score Breakdown

Violation Severity
70.8×40%
Refusal Volume
45.6×30%
Recency
87.2×20%
Frequency
6.9×10%
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

627×

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).

837×

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.

114×

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).

2743×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

2761×

PRESRV LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.

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.

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.

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.

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.

Refusal History

DateProductViolationsDivision
5/30/2025
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)
2/24/2012
27YCT99CONDIMENTS, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
2/24/2012
25ECP99MIXED VEGETABLES, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
2/24/2012
27YCT99CONDIMENTS, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
2/24/2012
21VCP05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
2/24/2012
37JCT05SOY SAUCE
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
2/24/2012
37JCT03CHILI SAUCE
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
10/16/2009
30BCT99FRUIT BEVERAGE BASES, LIQUID, N.E.C.
274COLOR LBLG
New York District Office (NYK-DO)
10/16/2009
30BCT99FRUIT BEVERAGE BASES, LIQUID, N.E.C.
274COLOR LBLG
New York District Office (NYK-DO)
10/16/2009
30BCT99FRUIT BEVERAGE BASES, LIQUID, N.E.C.
274COLOR LBLG
New York District Office (NYK-DO)
2/27/2004
37JCT08TOMATO SAUCE (WITH OTHER INGREDIENTS)
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Baltimore District Office (BLT-DO)
2/27/2004
21VYE19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
276PRESRV LBL
Baltimore District Office (BLT-DO)
1/15/2003
21RCT05MANGO (SUBTROPICAL AND TROPICAL FRUIT PUREES)
11UNSAFE COL
New York District Office (NYK-DO)
1/15/2003
36DCT99IMITATION SYRUPS, MOLASSES AND HONEY, N.E.C.
11UNSAFE COL
New York District Office (NYK-DO)
10/28/2002
37JCT99SAUCES, N.E.C.
11UNSAFE COL
62NEEDS FCE
New York District Office (NYK-DO)
5/15/2002
21VCT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
11UNSAFE COL
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Shezan International Limited's FDA import refusal history?

Shezan International Limited (FEI: 3010122553) has 16 FDA import refusal record(s) in our database, spanning from 5/15/2002 to 5/30/2025.

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. Shezan International Limited's FEI number is 3010122553.

What types of violations has Shezan International Limited received?

Shezan International Limited 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 Shezan International Limited come from?

All FDA import refusal data for Shezan International Limited 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.