Yarsons
⚠️ Moderate Risk
FEI: 3004708763 • Sialkot, Punjab • PAKISTAN
FEI Number
3004708763
Location
Sialkot, Punjab
Country
PAKISTANAddress
Khadim Ali 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
DEVICEGMPS
The article is subject to refusal of admission pursuant to Section 801(a)(1) in that the methods used in, or the facilities or controls used for, the manufacture, packing, storage, or installation of the device do not conform to the requirements of Section 520(f)(1) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) or a condition prescribed by an order under section 520(f)(2) of the FD&C Act.
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).
DE IMP GMP
The article is subject to refusal of admission pursuant to section 801(a)(1) in that it appears that the methods used in, or the facilities or controls used for, the manufacture of the device do not conform to the applicable requirements of section 520(f).
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).
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 |
|---|---|---|---|
| 11/30/2007 | 76EMDHEMOSTAT, SURGICAL | Chicago District Office (CHI-DO) | |
| 10/20/2005 | 85HCZFORCEPS, SURGICAL, GYNECOLOGICAL | 2780DEVICEGMPS | Florida District Office (FLA-DO) |
| 6/10/2005 | 85HDFSPECULUM, VAGINAL, METAL | 290DE IMP GMP | Division of Southeast Imports (DSEI) |
| 4/29/2005 | 85HCZFORCEPS, SURGICAL, GYNECOLOGICAL | Division of Southeast Imports (DSEI) | |
| 10/12/2004 | 85HCZFORCEPS, SURGICAL, GYNECOLOGICAL | Division of Southeast Imports (DSEI) | |
| 9/9/2004 | 85HDFSPECULUM, VAGINAL, METAL | 290DE IMP GMP | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Yarsons's FDA import refusal history?
Yarsons (FEI: 3004708763) has 6 FDA import refusal record(s) in our database, spanning from 9/9/2004 to 11/30/2007.
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. Yarsons's FEI number is 3004708763.
What types of violations has Yarsons received?
Yarsons 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 Yarsons come from?
All FDA import refusal data for Yarsons 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.