The Magstim Company Limited
⚠️ Moderate Risk
FEI: 3002808356 • Whitland, Dyfed • UNITED KINGDOM
FEI Number
3002808356
Location
Whitland, Dyfed
Country
UNITED KINGDOMAddress
Spring Gardens, , Whitland, Dyfed, 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 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/12/2021 | 84OBPTRANSCRANIAL MAGNETIC STIMULATOR | Division of West Coast Imports (DWCI) | |
| 2/12/2021 | 84OBPTRANSCRANIAL MAGNETIC STIMULATOR | Division of West Coast Imports (DWCI) | |
| 2/12/2021 | 84OBPTRANSCRANIAL MAGNETIC STIMULATOR | Division of West Coast Imports (DWCI) | |
| 10/2/2008 | 84NHINERVE, STIMULATOR, ELECTRICAL, PERCUTANEOUS (PENS) FOR PAIN RELIEF | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is The Magstim Company Limited's FDA import refusal history?
The Magstim Company Limited (FEI: 3002808356) has 4 FDA import refusal record(s) in our database, spanning from 10/2/2008 to 2/12/2021.
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. The Magstim Company Limited's FEI number is 3002808356.
What types of violations has The Magstim Company Limited received?
The Magstim Company Limited has been cited for 4 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 The Magstim Company Limited come from?
All FDA import refusal data for The Magstim Company 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.