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Kim Duong Co.

⚠️ Moderate Risk

FEI: 3004908904 • Tan Binh • VIETNAM

FEI

FEI Number

3004908904

📍

Location

Tan Binh

🇻🇳

Country

VIETNAM
🏢

Address

19/44/10 Bac Chai, Ward 6, Dist., , Tan Binh, , Vietnam

Moderate Risk

FDA Import Risk Assessment

34.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
11/13/2008
Latest Refusal
11/13/2008
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
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

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.

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

Refusal History

DateProductViolationsDivision
11/13/2008
25LGH25ONION BULB (YELLOW, WHITE, RED, ETC.), DRIED OR PASTE
249FILTHY
3320TRANSFAT
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Kim Duong Co.'s FDA import refusal history?

Kim Duong Co. (FEI: 3004908904) has 1 FDA import refusal record(s) in our database, spanning from 11/13/2008 to 11/13/2008.

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. Kim Duong Co.'s FEI number is 3004908904.

What types of violations has Kim Duong Co. received?

Kim Duong Co. 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 Kim Duong Co. come from?

All FDA import refusal data for Kim Duong Co. 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.