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HOKO CO.,LTD

⚠️ Moderate Risk

FEI: 3009228271 • Osaka, Osaka • JAPAN

FEI

FEI Number

3009228271

📍

Location

Osaka, Osaka

🇯🇵

Country

JAPAN
🏢

Address

6 Chome 2-1 Fukushima, Fukushima; Fukushima; Fukushima, Osaka, Osaka, Japan

Moderate Risk

FDA Import Risk Assessment

45.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
8/20/2003
Latest Refusal
5/1/2003
Earliest Refusal

Score Breakdown

Violation Severity
95.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2511×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
8/20/2003
16EGD03OYSTERS
308MFR INSAN
Los Angeles District Office (LOS-DO)
5/1/2003
16EGD03OYSTERS
251POISONOUS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

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

HOKO CO.,LTD (FEI: 3009228271) has 2 FDA import refusal record(s) in our database, spanning from 5/1/2003 to 8/20/2003.

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. HOKO CO.,LTD's FEI number is 3009228271.

What types of violations has HOKO CO.,LTD received?

HOKO CO.,LTD 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 HOKO CO.,LTD come from?

All FDA import refusal data for HOKO 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.