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MULTIMED INDUSTRIES

⚠️ Moderate Risk

FEI: 3021856271 • Sialkot • PAKISTAN

FEI

FEI Number

3021856271

📍

Location

Sialkot

🇵🇰

Country

PAKISTAN
🏢

Address

Mughal Pura Gohad Pur, , Sialkot, , Pakistan

Moderate Risk

FDA Import Risk Assessment

44.0
LowModerateHighCritical

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

Statistics

7
Total Refusals
4
Unique Violations
4/1/2022
Latest Refusal
4/1/2022
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
Refusal Volume
33.5×30%
Recency
10.0×20%
Frequency
70.0×10%
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

1187×

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).

2907×

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).

32807×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

5087×

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

DateProductViolationsDivision
4/1/2022
79LRWSCISSORS, GENERAL USE, SURGICAL
118NOT LISTED
290DE IMP GMP
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/1/2022
79GDZHANDLE, SCALPEL
118NOT LISTED
290DE IMP GMP
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/1/2022
79HTFCURETTE
118NOT LISTED
290DE IMP GMP
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/1/2022
79GADRETRACTOR, SURGICAL, GENERAL & PLASTIC SURGERY
118NOT LISTED
290DE IMP GMP
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/1/2022
79HXLMALLET
118NOT LISTED
290DE IMP GMP
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/1/2022
79GEGELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
118NOT LISTED
290DE IMP GMP
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/1/2022
79MDMINSTRUMENT, MANUAL, GENERAL SURGICAL
118NOT LISTED
290DE IMP GMP
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MULTIMED INDUSTRIES's FDA import refusal history?

MULTIMED INDUSTRIES (FEI: 3021856271) has 7 FDA import refusal record(s) in our database, spanning from 4/1/2022 to 4/1/2022.

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. MULTIMED INDUSTRIES's FEI number is 3021856271.

What types of violations has MULTIMED INDUSTRIES received?

MULTIMED INDUSTRIES 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 MULTIMED INDUSTRIES come from?

All FDA import refusal data for MULTIMED INDUSTRIES 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.