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Agripina Dak

⚠️ High Risk

FEI: 3004752081 • Moscow, Moscow g • RUSSIA

FEI

FEI Number

3004752081

📍

Location

Moscow, Moscow g

🇷🇺

Country

RUSSIA
🏢

Address

Pestovskiy per 121, , Moscow, Moscow g, Russia

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
11/10/2004
Latest Refusal
11/10/2004
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2494×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
11/10/2004
16LGP01CRAB, CAKES, BALLS, ETC.
249FILTHY
New York District Office (NYK-DO)
11/10/2004
16LGP01CRAB, CAKES, BALLS, ETC.
249FILTHY
New York District Office (NYK-DO)
11/10/2004
16LGP01CRAB, CAKES, BALLS, ETC.
249FILTHY
New York District Office (NYK-DO)
11/10/2004
16LGP01CRAB, CAKES, BALLS, ETC.
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is Agripina Dak's FDA import refusal history?

Agripina Dak (FEI: 3004752081) has 4 FDA import refusal record(s) in our database, spanning from 11/10/2004 to 11/10/2004.

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. Agripina Dak's FEI number is 3004752081.

What types of violations has Agripina Dak received?

Agripina Dak 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 Agripina Dak come from?

All FDA import refusal data for Agripina Dak 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.