Sony Europa
⚠️ Moderate Risk
FEI: 3002367945 • Badhoevedorp, Noord-Holland • NETHERLANDS
FEI Number
3002367945
Location
Badhoevedorp, Noord-Holland
Country
NETHERLANDSAddress
Schipholweg 275, , Badhoevedorp, Noord-Holland, Netherlands
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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).
FAILS STD
The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/17/2007 | 95L31CD PLAYERS (COMPACT DISC PLAYERS) | 476NO REGISTR | Baltimore District Office (BLT-DO) |
| 4/17/2007 | 95L31CD PLAYERS (COMPACT DISC PLAYERS) | 476NO REGISTR | Baltimore District Office (BLT-DO) |
| 4/17/2007 | 95L31CD PLAYERS (COMPACT DISC PLAYERS) | 126FAILS STD | Baltimore District Office (BLT-DO) |
| 10/2/2006 | 95L31CD PLAYERS (COMPACT DISC PLAYERS) | 476NO REGISTR | Baltimore District Office (BLT-DO) |
| 10/2/2006 | 95L31CD PLAYERS (COMPACT DISC PLAYERS) | 47NON STD | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Sony Europa's FDA import refusal history?
Sony Europa (FEI: 3002367945) has 5 FDA import refusal record(s) in our database, spanning from 10/2/2006 to 4/17/2007.
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 Europa's FEI number is 3002367945.
What types of violations has Sony Europa received?
Sony Europa has been cited for 3 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 Europa come from?
All FDA import refusal data for Sony Europa 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.