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ONOMICHI ENKAN CO., LTD.

⚠️ Moderate Risk

FEI: 3004266001 • Onomichi-shi, Hiroshima-ken • JAPAN

FEI

FEI Number

3004266001

📍

Location

Onomichi-shi, Hiroshima-ken

🇯🇵

Country

JAPAN
🏢

Address

7 14 Higashionomichi, , Onomichi-shi, Hiroshima-ken, Japan

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
5/2/2012
Latest Refusal
5/2/2012
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

3062×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
5/2/2012
16AFH01ANCHOVY
306INSANITARY
Los Angeles District Office (LOS-DO)
5/2/2012
16AFH01ANCHOVY
306INSANITARY
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

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

ONOMICHI ENKAN CO., LTD. (FEI: 3004266001) has 2 FDA import refusal record(s) in our database, spanning from 5/2/2012 to 5/2/2012.

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. ONOMICHI ENKAN CO., LTD.'s FEI number is 3004266001.

What types of violations has ONOMICHI ENKAN CO., LTD. received?

ONOMICHI ENKAN 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 ONOMICHI ENKAN CO., LTD. come from?

All FDA import refusal data for ONOMICHI ENKAN 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.