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MEDZONE INSTRUMENT

⚠️ High Risk

FEI: 3035556964 • West Sialkot • PAKISTAN

FEI

FEI Number

3035556964

📍

Location

West Sialkot

🇵🇰

Country

PAKISTAN
🏢

Address

New Miana Pura Roras Rd, , West Sialkot, , Pakistan

High Risk

FDA Import Risk Assessment

53.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

1
Total Refusals
1
Unique Violations
4/2/2025
Latest Refusal
4/2/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
84.2×20%
Frequency
10.0×10%
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

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
4/2/2025
76JETPICK, MASSAGING
290DE IMP GMP
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MEDZONE INSTRUMENT's FDA import refusal history?

MEDZONE INSTRUMENT (FEI: 3035556964) has 1 FDA import refusal record(s) in our database, spanning from 4/2/2025 to 4/2/2025.

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. MEDZONE INSTRUMENT's FEI number is 3035556964.

What types of violations has MEDZONE INSTRUMENT received?

MEDZONE INSTRUMENT has been cited for 1 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 MEDZONE INSTRUMENT come from?

All FDA import refusal data for MEDZONE INSTRUMENT 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.