The Mughal Surgical (Pvt) Ltd.
⚠️ Moderate Risk
FEI: 3003186984 • Sialkot, Punjab • PAKISTAN
FEI Number
3003186984
Location
Sialkot, Punjab
Country
PAKISTANAddress
C-95 Industrial Estate, , 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).
DV QUALITY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/3/2011 | 78FGMPROBE AND DIRECTOR, GASTRO-UROLOGY | 2780DEVICEGMPS | Philadelphia District Office (PHI-DO) |
| 1/3/2011 | 87HXKHOLDER, NEEDLE; ORTHOPEDIC | 2780DEVICEGMPS | Philadelphia District Office (PHI-DO) |
| 1/3/2011 | 79LRWSCISSORS, GENERAL USE, SURGICAL | 2780DEVICEGMPS | Philadelphia District Office (PHI-DO) |
| 1/3/2011 | 79GENFORCEPS, GENERAL & PLASTIC SURGERY | 2780DEVICEGMPS | Philadelphia District Office (PHI-DO) |
| 9/16/2010 | 79HTDFORCEPS | 290DE IMP GMP | New Orleans District Office (NOL-DO) |
| 5/14/2010 | 76JEXPLIER, ORTHODONTIC | Philadelphia District Office (PHI-DO) | |
| 3/11/2003 | 77JZFTUBE, EAR SUCTION | 118NOT LISTED | New York District Office (NYK-DO) |
| 3/11/2003 | 79HXMRETRACTOR | 118NOT LISTED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is The Mughal Surgical (Pvt) Ltd.'s FDA import refusal history?
The Mughal Surgical (Pvt) Ltd. (FEI: 3003186984) has 8 FDA import refusal record(s) in our database, spanning from 3/11/2003 to 1/3/2011.
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. The Mughal Surgical (Pvt) Ltd.'s FEI number is 3003186984.
What types of violations has The Mughal Surgical (Pvt) Ltd. received?
The Mughal Surgical (Pvt) Ltd. 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 The Mughal Surgical (Pvt) Ltd. come from?
All FDA import refusal data for The Mughal Surgical (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.