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Spectrum Surgical Supplies

⚠️ Moderate Risk

FEI: 3005374323 • SIALKOT, PUNJAB • PAKISTAN

FEI

FEI Number

3005374323

📍

Location

SIALKOT, PUNJAB

🇵🇰

Country

PAKISTAN
🏢

Address

4/33 Ch. Fazal Din Street, Ahmedpura, SIALKOT, PUNJAB, Pakistan

Moderate Risk

FDA Import Risk Assessment

37.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

4
Total Refusals
5
Unique Violations
9/26/2006
Latest Refusal
10/21/2005
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2902×

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).

1181×

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).

27801×

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.

3411×

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).

4801×

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

DateProductViolationsDivision
9/26/2006
79GENFORCEPS, GENERAL & PLASTIC SURGERY
480STAINSTEEL
New York District Office (NYK-DO)
12/13/2005
85HCZFORCEPS, SURGICAL, GYNECOLOGICAL
118NOT LISTED
2780DEVICEGMPS
341REGISTERED
New York District Office (NYK-DO)
11/7/2005
85HDFSPECULUM, VAGINAL, METAL
290DE IMP GMP
New York District Office (NYK-DO)
10/21/2005
85HDFSPECULUM, VAGINAL, METAL
290DE IMP GMP
New York District Office (NYK-DO)

Frequently Asked Questions

What is Spectrum Surgical Supplies's FDA import refusal history?

Spectrum Surgical Supplies (FEI: 3005374323) has 4 FDA import refusal record(s) in our database, spanning from 10/21/2005 to 9/26/2006.

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. Spectrum Surgical Supplies's FEI number is 3005374323.

What types of violations has Spectrum Surgical Supplies received?

Spectrum Surgical Supplies 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 Spectrum Surgical Supplies come from?

All FDA import refusal data for Spectrum Surgical Supplies 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.