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KOK GEE GAN

⚠️ Moderate Risk

FEI: 3026957507 • Kuala Lumpur, WP Kuala Lumpur • MALAYSIA

FEI

FEI Number

3026957507

📍

Location

Kuala Lumpur, WP Kuala Lumpur

🇲🇾

Country

MALAYSIA
🏢

Address

17 Lorong Ayer Bersih 3, 3tmn Air Pan, Kuala Lumpur, WP Kuala Lumpur, Malaysia

Moderate Risk

FDA Import Risk Assessment

34.9
LowModerateHighCritical

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

Statistics

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

Score Breakdown

Violation Severity
36.7×40%
Refusal Volume
22.3×30%
Recency
52.9×20%
Frequency
30.0×10%
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

2183×

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.

23003×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

3203×

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.

Refusal History

DateProductViolationsDivision
6/4/2024
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
Division of Southeast Imports (DSEI)
6/4/2024
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
Division of Southeast Imports (DSEI)
6/4/2024
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is KOK GEE GAN's FDA import refusal history?

KOK GEE GAN (FEI: 3026957507) has 3 FDA import refusal record(s) in our database, spanning from 6/4/2024 to 6/4/2024.

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. KOK GEE GAN's FEI number is 3026957507.

What types of violations has KOK GEE GAN received?

KOK GEE GAN 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 KOK GEE GAN come from?

All FDA import refusal data for KOK GEE GAN 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.