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Imp Japan, Inc.

⚠️ Moderate Risk

FEI: 3007421211 • Chuo, Tokyo • JAPAN

FEI

FEI Number

3007421211

📍

Location

Chuo, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

8-19, Toyomi-Cho, Chuo, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
1/6/2014
Latest Refusal
11/21/2013
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

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).

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
1/6/2014
25JGP24GINGER ROOT (ROOT & TUBER VEGETABLE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
11/21/2013
25JGP07RADISH (ROOT & TUBER VEGETABLE)
64YELLOW #5
San Francisco District Office (SAN-DO)
11/21/2013
25JGP24GINGER ROOT (ROOT & TUBER VEGETABLE)
11UNSAFE COL
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Imp Japan, Inc.'s FDA import refusal history?

Imp Japan, Inc. (FEI: 3007421211) has 3 FDA import refusal record(s) in our database, spanning from 11/21/2013 to 1/6/2014.

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. Imp Japan, Inc.'s FEI number is 3007421211.

What types of violations has Imp Japan, Inc. received?

Imp Japan, Inc. 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 Imp Japan, Inc. come from?

All FDA import refusal data for Imp Japan, Inc. 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.