ImportRefusal LogoImportRefusal

H.A.CO.,LTD.

⚠️ High Risk

FEI: 3027471573 • Cheongdo, Gyeongsangbuk • SOUTH KOREA

FEI

FEI Number

3027471573

📍

Location

Cheongdo, Gyeongsangbuk

🇰🇷
🏢

Address

107 Haksan1-Gil, Iseo-Myeon, Cheongdo, Gyeongsangbuk, South Korea

High Risk

FDA Import Risk Assessment

66.3
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
5/27/2025
Latest Refusal
4/9/2025
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
72.7×20%
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

2954×

LISTERIA

The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.

Refusal History

DateProductViolationsDivision
5/27/2025
25SGC14ENOKITAKE
295LISTERIA
Division of West Coast Imports (DWCI)
5/27/2025
25SGC14ENOKITAKE
295LISTERIA
Division of West Coast Imports (DWCI)
4/9/2025
25SGC14ENOKITAKE
295LISTERIA
Division of West Coast Imports (DWCI)
4/9/2025
25SGC14ENOKITAKE
295LISTERIA
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is H.A.CO.,LTD.'s FDA import refusal history?

H.A.CO.,LTD. (FEI: 3027471573) has 4 FDA import refusal record(s) in our database, spanning from 4/9/2025 to 5/27/2025.

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. H.A.CO.,LTD.'s FEI number is 3027471573.

What types of violations has H.A.CO.,LTD. received?

H.A.CO.,LTD. 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 H.A.CO.,LTD. come from?

All FDA import refusal data for H.A.CO.,LTD. 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.