Nurikon International (Pvt) Ltd.
⚠️ Moderate Risk
FEI: 1000403938 • Sialkot, Punjab • PAKISTAN
FEI Number
1000403938
Location
Sialkot, Punjab
Country
PAKISTANAddress
Sakina House - Nasir Road, , Sialkot, Punjab, Pakistan
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
STAINSTEEL
The article appears to be a device whose quality falls below that which it purports or is represented to possess, in that instrument is represented as stainless steel but does not meet requirements for such steel for surgical instruments.
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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/25/2015 | 76EGNSCISSORS, SURGICAL TISSUE, DENTAL | 341REGISTERED | Florida District Office (FLA-DO) |
| 8/25/2015 | 76JEXPLIER, ORTHODONTIC | 341REGISTERED | Florida District Office (FLA-DO) |
| 3/14/2003 | 79LRWSCISSORS, GENERAL USE, SURGICAL | 480STAINSTEEL | New York District Office (NYK-DO) |
| 3/14/2003 | 84HAOINSTRUMENT, SURGICAL, NON-POWERED | 480STAINSTEEL | New York District Office (NYK-DO) |
| 3/14/2003 | 84HAOINSTRUMENT, SURGICAL, NON-POWERED | 480STAINSTEEL | New York District Office (NYK-DO) |
| 3/14/2003 | 79GANSUTURE, ABSORBABLE, SYNTHETIC | 480STAINSTEEL | New York District Office (NYK-DO) |
| 3/22/2002 | 79MDWINSTRUMENT, MANUAL, SURGICAL, GENERAL USE | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Nurikon International (Pvt) Ltd.'s FDA import refusal history?
Nurikon International (Pvt) Ltd. (FEI: 1000403938) has 7 FDA import refusal record(s) in our database, spanning from 3/22/2002 to 8/25/2015.
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. Nurikon International (Pvt) Ltd.'s FEI number is 1000403938.
What types of violations has Nurikon International (Pvt) Ltd. received?
Nurikon International (Pvt) Ltd. 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 Nurikon International (Pvt) Ltd. come from?
All FDA import refusal data for Nurikon International (Pvt) 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.