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Dalmore Product

⚠️ Moderate Risk

FEI: 3003219615 • Vladivostok, Primorskiy kray • RUSSIA

FEI

FEI Number

3003219615

📍

Location

Vladivostok, Primorskiy kray

🇷🇺

Country

RUSSIA
🏢

Address

ul. Fontannaya 24, , Vladivostok, Primorskiy kray, Russia

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
10/16/2001
Latest Refusal
10/16/2001
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
10/16/2001
16YEE01CAVIAR, FISHERY PRODUCTS, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
10/16/2001
16MEE03SQUID, OTHER AQUATIC SPECIES
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Dalmore Product's FDA import refusal history?

Dalmore Product (FEI: 3003219615) has 2 FDA import refusal record(s) in our database, spanning from 10/16/2001 to 10/16/2001.

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. Dalmore Product's FEI number is 3003219615.

What types of violations has Dalmore Product received?

Dalmore Product 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 Dalmore Product come from?

All FDA import refusal data for Dalmore Product 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.