Top Glovel SDN. BHD.
⚠️ Moderate Risk
FEI: 1000602471 • Kapar, Selangor • MALAYSIA
FEI Number
1000602471
Location
Kapar, Selangor
Country
MALAYSIAAddress
Kapar, 24 Jalan Raja Mokhtar, Kapar, Selangor, Malaysia
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.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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.
HOLES
The quality of the article falls below that which it purports or is represented to possess, in that the devices contain defects/holes.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/14/2015 | 79KGOSURGEON'S GLOVES | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 9/14/2015 | 79KGOSURGEON'S GLOVES | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 3/20/2015 | 80LZAGLOVE, PATIENT EXAMINATION, POLY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 2/13/2015 | 79KGOSURGEON'S GLOVES | Division of Southeast Imports (DSEI) | |
| 1/26/2015 | 80LYYGLOVE, PATIENT EXAMINATION, LATEX | Division of Southeast Imports (DSEI) | |
| 8/22/2014 | 80LYYGLOVE, PATIENT EXAMINATION, LATEX | Division of Southeast Imports (DSEI) | |
| 1/17/2007 | 79KGOSURGEON'S GLOVES | Division of Southeast Imports (DSEI) | |
| 1/4/2007 | 79KGOSURGEON'S GLOVES | Florida District Office (FLA-DO) | |
| 11/27/2006 | 80LYYGLOVE, PATIENT EXAMINATION, LATEX | Florida District Office (FLA-DO) | |
| 11/27/2006 | 80LYYGLOVE, PATIENT EXAMINATION, LATEX | Florida District Office (FLA-DO) | |
| 11/27/2006 | 80LYYGLOVE, PATIENT EXAMINATION, LATEX | Florida District Office (FLA-DO) | |
| 7/8/2003 | 80LYYGLOVE, PATIENT EXAMINATION, LATEX | 477HOLES | New York District Office (NYK-DO) |
| 6/6/2003 | 80LYYGLOVE, PATIENT EXAMINATION, LATEX | 477HOLES | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Top Glovel SDN. BHD.'s FDA import refusal history?
Top Glovel SDN. BHD. (FEI: 1000602471) has 13 FDA import refusal record(s) in our database, spanning from 6/6/2003 to 9/14/2015.
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. Top Glovel SDN. BHD.'s FEI number is 1000602471.
What types of violations has Top Glovel SDN. BHD. received?
Top Glovel SDN. BHD. has been cited for 5 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 Top Glovel SDN. BHD. come from?
All FDA import refusal data for Top Glovel SDN. BHD. 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.