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Dai Tien Vinh Company

⚠️ High Risk

FEI: 3011289714 • Vung Tau, Ba Ria-Vung Tau • VIETNAM

FEI

FEI Number

3011289714

📍

Location

Vung Tau, Ba Ria-Vung Tau

🇻🇳

Country

VIETNAM
🏢

Address

1717a Vo Nguyen Giap Street, Ward 12, Vung Tau, Ba Ria-Vung Tau, Vietnam

High Risk

FDA Import Risk Assessment

57.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
8/8/2024
Latest Refusal
8/8/2024
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
56.6×20%
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

23603×

HISTAMINE

The article appears to bear or contain histamine, a poisonous and deleterious substance in such quantity as ordinarily renders it injurious to health.

Refusal History

DateProductViolationsDivision
8/8/2024
16AVD45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Division of West Coast Imports (DWCI)
8/8/2024
16AVD45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Division of West Coast Imports (DWCI)
8/8/2024
16AVD45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Dai Tien Vinh Company's FDA import refusal history?

Dai Tien Vinh Company (FEI: 3011289714) has 3 FDA import refusal record(s) in our database, spanning from 8/8/2024 to 8/8/2024.

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. Dai Tien Vinh Company's FEI number is 3011289714.

What types of violations has Dai Tien Vinh Company received?

Dai Tien Vinh Company has been cited for 1 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 Dai Tien Vinh Company come from?

All FDA import refusal data for Dai Tien Vinh Company 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.