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Amk Market

⚠️ Moderate Risk

FEI: 3003392924 • Moscow, Moscow g • RUSSIA

FEI

FEI Number

3003392924

📍

Location

Moscow, Moscow g

🇷🇺

Country

RUSSIA
🏢

Address

ul. Dnepropetrovskaya 5, , Moscow, Moscow g, Russia

Moderate Risk

FDA Import Risk Assessment

49.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
1
Unique Violations
9/14/2004
Latest Refusal
6/2/2004
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

755×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
9/14/2004
66VBA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
9/14/2004
66VBA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
6/15/2004
66VBA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of West Coast Imports (DWCI)
6/2/2004
66VBA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Los Angeles District Office (LOS-DO)
6/2/2004
66VBA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Amk Market's FDA import refusal history?

Amk Market (FEI: 3003392924) has 5 FDA import refusal record(s) in our database, spanning from 6/2/2004 to 9/14/2004.

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. Amk Market's FEI number is 3003392924.

What types of violations has Amk Market received?

Amk Market 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 Amk Market come from?

All FDA import refusal data for Amk Market 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.