Unipart Exports Limited
⚠️ Moderate Risk
FEI: 1000381841 • Oxford • UNITED KINGDOM
FEI Number
1000381841
Location
Oxford
Country
UNITED KINGDOMAddress
Unipart House, 2nd Floor East; Garsington Road, Oxford, , United Kingdom
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/20/2004 | 95L32CD PLAYER COMBINATION SYSTEMS | 476NO REGISTR | New York District Office (NYK-DO) |
| 10/20/2004 | 95L32CD PLAYER COMBINATION SYSTEMS | 476NO REGISTR | New York District Office (NYK-DO) |
| 7/10/2003 | 95L31CD PLAYERS (COMPACT DISC PLAYERS) | 126FAILS STD | Atlanta District Office (ATL-DO) |
| 5/2/2002 | 95L31CD PLAYERS (COMPACT DISC PLAYERS) | 476NO REGISTR | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Unipart Exports Limited's FDA import refusal history?
Unipart Exports Limited (FEI: 1000381841) has 4 FDA import refusal record(s) in our database, spanning from 5/2/2002 to 10/20/2004.
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. Unipart Exports Limited's FEI number is 1000381841.
What types of violations has Unipart Exports Limited received?
Unipart Exports Limited 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 Unipart Exports Limited come from?
All FDA import refusal data for Unipart Exports Limited 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.