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Karmanwala International

⚠️ Moderate Risk

FEI: 3009638977 • Okara, Punjab • PAKISTAN

FEI

FEI Number

3009638977

📍

Location

Okara, Punjab

🇵🇰

Country

PAKISTAN
🏢

Address

Grain Market, , Okara, Punjab, Pakistan

Moderate Risk

FDA Import Risk Assessment

38.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
3
Unique Violations
5/24/2016
Latest Refusal
5/3/2016
Earliest Refusal

Score Breakdown

Violation Severity
67.5×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2414×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

2562×

INCONSPICU

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)).

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.

Refusal History

DateProductViolationsDivision
5/24/2016
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
241PESTICIDE
Division of Northeast Imports (DNEI)
5/24/2016
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
241PESTICIDE
New York District Office (NYK-DO)
5/3/2016
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
241PESTICIDE
256INCONSPICU
482NUTRIT LBL
Division of West Coast Imports (DWCI)
5/3/2016
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
241PESTICIDE
256INCONSPICU
482NUTRIT LBL
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Karmanwala International's FDA import refusal history?

Karmanwala International (FEI: 3009638977) has 4 FDA import refusal record(s) in our database, spanning from 5/3/2016 to 5/24/2016.

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. Karmanwala International's FEI number is 3009638977.

What types of violations has Karmanwala International received?

Karmanwala International has been cited for 3 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 Karmanwala International come from?

All FDA import refusal data for Karmanwala International 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.