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Kentwe Products (M) SDN. BHD.

⚠️ Moderate Risk

FEI: 3004285196 • MASJID TANAH, MY-M • MALAYSIA

FEI

FEI Number

3004285196

📍

Location

MASJID TANAH, MY-M

🇲🇾

Country

MALAYSIA
🏢

Address

St 524, Lot A1,, Kaw Ind Miel, Pengkalan Balak, MASJID TANAH, MY-M, Malaysia

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
5/18/2009
Latest Refusal
5/18/2009
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

28601×

VETDRUGRES

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains

Refusal History

DateProductViolationsDivision
5/18/2009
36CET04HONEY
238UNSAFE ADD
2860VETDRUGRES
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Kentwe Products (M) SDN. BHD.'s FDA import refusal history?

Kentwe Products (M) SDN. BHD. (FEI: 3004285196) has 1 FDA import refusal record(s) in our database, spanning from 5/18/2009 to 5/18/2009.

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. Kentwe Products (M) SDN. BHD.'s FEI number is 3004285196.

What types of violations has Kentwe Products (M) SDN. BHD. received?

Kentwe Products (M) SDN. BHD. has been cited for 2 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 Kentwe Products (M) SDN. BHD. come from?

All FDA import refusal data for Kentwe Products (M) SDN. BHD. 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.