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Nozaki Tsukemono Company

⚠️ Moderate Risk

FEI: 9839 • Miyazaki • JAPAN

FEI

FEI Number

9839

📍

Location

Miyazaki

🇯🇵

Country

JAPAN
🏢

Address

102 Daiwa Cho, , Miyazaki, , Japan

Moderate Risk

FDA Import Risk Assessment

36.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
11/16/2004
Latest Refusal
9/4/2002
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
9.1×10%
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

111×

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).

641×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

Refusal History

DateProductViolationsDivision
11/16/2004
25NGT07RADISH, WITH SAUCE
64YELLOW #5
New York District Office (NYK-DO)
9/4/2002
25JGP07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Nozaki Tsukemono Company's FDA import refusal history?

Nozaki Tsukemono Company (FEI: 9839) has 2 FDA import refusal record(s) in our database, spanning from 9/4/2002 to 11/16/2004.

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. Nozaki Tsukemono Company's FEI number is 9839.

What types of violations has Nozaki Tsukemono Company received?

Nozaki Tsukemono Company 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 Nozaki Tsukemono Company come from?

All FDA import refusal data for Nozaki Tsukemono 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.