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Glorious Mercantile Corp. Pvt. Ltd.

⚠️ Moderate Risk

FEI: 1000555370 • Sialkot • PAKISTAN

FEI

FEI Number

1000555370

📍

Location

Sialkot

🇵🇰

Country

PAKISTAN
🏢

Address

15-a-Small Industrial Estate, , Sialkot, , Pakistan

Moderate Risk

FDA Import Risk Assessment

37.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
6/7/2007
Latest Refusal
9/17/2004
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
11.0×10%
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

2261×

DEVICE GMP

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.

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.

2901×

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).

Refusal History

DateProductViolationsDivision
6/7/2007
79LRWSCISSORS, GENERAL USE, SURGICAL
2780DEVICEGMPS
Southwest Import District Office (SWI-DO)
6/7/2007
79LRWSCISSORS, GENERAL USE, SURGICAL
226DEVICE GMP
Southwest Import District Office (SWI-DO)
9/17/2004
79HTDFORCEPS
290DE IMP GMP
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Glorious Mercantile Corp. Pvt. Ltd.'s FDA import refusal history?

Glorious Mercantile Corp. Pvt. Ltd. (FEI: 1000555370) has 3 FDA import refusal record(s) in our database, spanning from 9/17/2004 to 6/7/2007.

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. Glorious Mercantile Corp. Pvt. Ltd.'s FEI number is 1000555370.

What types of violations has Glorious Mercantile Corp. Pvt. Ltd. received?

Glorious Mercantile Corp. Pvt. Ltd. has been cited for 3 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 Glorious Mercantile Corp. Pvt. Ltd. come from?

All FDA import refusal data for Glorious Mercantile Corp. 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.