Laurence Dunne
⚠️ High Risk
FEI: 3006095095 • Surrey • UNITED KINGDOM
FEI Number
3006095095
Location
Surrey
Country
UNITED KINGDOMAddress
218 Brighton Rd, , Surrey, , United Kingdom
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/5/2007 | 64UCB06FINASTERIDE (INHIBITOR (DECARBOXYLASE)) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 3/5/2007 | 65PCB03TAMSULOSIN HCL (REGULATOR) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 3/5/2007 | 62GAO99ANTI-INFLAMMATORY N.E.C. | 75UNAPPROVED | New York District Office (NYK-DO) |
| 3/5/2007 | 60XAK26LEVOBUNOLOL HYDROCHLORIDE (ANTI-ADRENERGIC) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 3/5/2007 | 60LAE56PROPOXYPHENE HCL (ANALGESIC) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 3/5/2007 | 60XCF17ATENOLOL (ANTI-ADRENERGIC) | 75UNAPPROVED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Laurence Dunne's FDA import refusal history?
Laurence Dunne (FEI: 3006095095) has 6 FDA import refusal record(s) in our database, spanning from 3/5/2007 to 3/5/2007.
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. Laurence Dunne's FEI number is 3006095095.
What types of violations has Laurence Dunne received?
Laurence Dunne has been cited for 1 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 Laurence Dunne come from?
All FDA import refusal data for Laurence Dunne 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.