Cuxson Gerrard & Co. Ltd.
⚠️ Moderate Risk
FEI: 3003132519 • Oldbury, West Midlands • UNITED KINGDOM
FEI Number
3003132519
Location
Oldbury, West Midlands
Country
UNITED KINGDOMAddress
125 Broadwell Road, , Oldbury, West Midlands, 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/24/2011 | 61KAJ06BELLADONNA (EXT) (ANTI-CHOLINERGIC) | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/6/2007 | 89MOCCUSHION, FLOTATION, THERAPEUTIC | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/27/2006 | 89MVTINSOLES, MAGNETIC, THERAPY, SUPPORTS | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 2/12/2002 | 79KGXTAPE AND BANDAGE, ADHESIVE | 118NOT LISTED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Cuxson Gerrard & Co. Ltd.'s FDA import refusal history?
Cuxson Gerrard & Co. Ltd. (FEI: 3003132519) has 4 FDA import refusal record(s) in our database, spanning from 2/12/2002 to 8/24/2011.
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. Cuxson Gerrard & Co. Ltd.'s FEI number is 3003132519.
What types of violations has Cuxson Gerrard & Co. Ltd. received?
Cuxson Gerrard & Co. Ltd. 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 Cuxson Gerrard & Co. Ltd. come from?
All FDA import refusal data for Cuxson Gerrard & Co. Ltd. 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.