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Andromeda Enterprises

⚠️ Moderate Risk

FEI: 3006481766 • Behram • PAKISTAN

FEI

FEI Number

3006481766

📍

Location

Behram

🇵🇰

Country

PAKISTAN
🏢

Address

Airport Road Chowk, , Behram, , Pakistan

Moderate Risk

FDA Import Risk Assessment

41.6
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
4/20/2009
Latest Refusal
4/14/2008
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
29.5×10%
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

2903×

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
4/20/2009
79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
290DE IMP GMP
Cincinnati District Office (CIN-DO)
4/14/2008
79GENFORCEPS, GENERAL & PLASTIC SURGERY
290DE IMP GMP
Cincinnati District Office (CIN-DO)
4/14/2008
79GENFORCEPS, GENERAL & PLASTIC SURGERY
290DE IMP GMP
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Andromeda Enterprises's FDA import refusal history?

Andromeda Enterprises (FEI: 3006481766) has 3 FDA import refusal record(s) in our database, spanning from 4/14/2008 to 4/20/2009.

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. Andromeda Enterprises's FEI number is 3006481766.

What types of violations has Andromeda Enterprises received?

Andromeda Enterprises 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 Andromeda Enterprises come from?

All FDA import refusal data for Andromeda Enterprises 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.