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Tenco Shokuhin Kogyo Kk

⚠️ Moderate Risk

FEI: 1000169682 • Aichi-Ken • JAPAN

FEI

FEI Number

1000169682

📍

Location

Aichi-Ken

🇯🇵

Country

JAPAN
🏢

Address

1-1 Hachimai-Mono, , Aichi-Ken, , Japan

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
5/11/2012
Latest Refusal
5/11/2012
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
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

114×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
5/11/2012
25JGP24GINGER ROOT (ROOT & TUBER VEGETABLE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
5/11/2012
25JGP24GINGER ROOT (ROOT & TUBER VEGETABLE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
5/11/2012
25JGP24GINGER ROOT (ROOT & TUBER VEGETABLE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
5/11/2012
25JGP24GINGER ROOT (ROOT & TUBER VEGETABLE)
11UNSAFE COL
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Tenco Shokuhin Kogyo Kk's FDA import refusal history?

Tenco Shokuhin Kogyo Kk (FEI: 1000169682) has 4 FDA import refusal record(s) in our database, spanning from 5/11/2012 to 5/11/2012.

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. Tenco Shokuhin Kogyo Kk's FEI number is 1000169682.

What types of violations has Tenco Shokuhin Kogyo Kk received?

Tenco Shokuhin Kogyo Kk 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 Tenco Shokuhin Kogyo Kk come from?

All FDA import refusal data for Tenco Shokuhin Kogyo Kk 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.