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MIYAMAE CO.,LTD

⚠️ Moderate Risk

FEI: 3004248137 • Ikoma-Gun, Nara • JAPAN

FEI

FEI Number

3004248137

📍

Location

Ikoma-Gun, Nara

🇯🇵

Country

JAPAN
🏢

Address

2 Chome 12-36, Nishinomiya; Heguri-Cho, Ikoma-Gun, Nara, Japan

Moderate Risk

FDA Import Risk Assessment

37.3
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
6/23/2015
Latest Refusal
1/23/2013
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
12.4×10%
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

112×

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).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
6/23/2015
25JGT24GINGER ROOT (ROOT & TUBER VEGETABLE)
473LABELING
Los Angeles District Office (LOS-DO)
1/31/2013
28AGP19GINGER, WHOLE (SPICE)
11UNSAFE COL
Division of West Coast Imports (DWCI)
1/23/2013
28AGP19GINGER, WHOLE (SPICE)
11UNSAFE COL
San Francisco District Office (SAN-DO)

Frequently Asked Questions

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

MIYAMAE CO.,LTD (FEI: 3004248137) has 3 FDA import refusal record(s) in our database, spanning from 1/23/2013 to 6/23/2015.

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. MIYAMAE CO.,LTD's FEI number is 3004248137.

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

MIYAMAE 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 MIYAMAE CO.,LTD come from?

All FDA import refusal data for MIYAMAE 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.