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Sony Corporation

⚠️ Moderate Risk

FEI: 1000546486 • Shinagawa, Tokyo • JAPAN

FEI

FEI Number

1000546486

📍

Location

Shinagawa, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

Shinagawa-Ku-Tokyo Japan, 2 Chome 10-14; Osaki, Shinagawa, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

31.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
4/8/2011
Latest Refusal
10/17/2003
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
2.7×10%
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

471×

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.

4761×

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
4/8/2011
94RBEVIDEO MONITOR, GENERAL PURPOSE, COLOR
476NO REGISTR
San Francisco District Office (SAN-DO)
10/17/2003
94V05CATHODE RAY TUBE
47NON STD
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Sony Corporation's FDA import refusal history?

Sony Corporation (FEI: 1000546486) has 2 FDA import refusal record(s) in our database, spanning from 10/17/2003 to 4/8/2011.

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. Sony Corporation's FEI number is 1000546486.

What types of violations has Sony Corporation received?

Sony Corporation 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 Sony Corporation come from?

All FDA import refusal data for Sony Corporation 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.