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Marantz Japan

⚠️ Moderate Risk

FEI: 1000191755 • Kanagawa • JAPAN

FEI

FEI Number

1000191755

📍

Location

Kanagawa

🇯🇵

Country

JAPAN
🏢

Address

35-1 7-Chome, Sagamiono, Kanagawa, , Japan

Moderate Risk

FDA Import Risk Assessment

33.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
6/17/2003
Latest Refusal
1/30/2003
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

472×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

4762×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
6/17/2003
95L31CD PLAYERS (COMPACT DISC PLAYERS)
47NON STD
476NO REGISTR
Chicago District Office (CHI-DO)
1/30/2003
95L31CD PLAYERS (COMPACT DISC PLAYERS)
47NON STD
476NO REGISTR
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Marantz Japan's FDA import refusal history?

Marantz Japan (FEI: 1000191755) has 2 FDA import refusal record(s) in our database, spanning from 1/30/2003 to 6/17/2003.

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. Marantz Japan's FEI number is 1000191755.

What types of violations has Marantz Japan received?

Marantz Japan 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 Marantz Japan come from?

All FDA import refusal data for Marantz Japan 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.