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Brivais Vilnis

⚠️ Moderate Risk

FEI: 3002668627 • Salacgriva, Salacgrivas Novads • LATVIA

FEI

FEI Number

3002668627

📍

Location

Salacgriva, Salacgrivas Novads

🇱🇻

Country

LATVIA
🏢

Address

Ostas Iela 1, , Salacgriva, Salacgrivas Novads, Latvia

Moderate Risk

FDA Import Risk Assessment

40.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
8/5/2005
Latest Refusal
5/3/2002
Earliest Refusal

Score Breakdown

Violation Severity
78.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
12.3×10%
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

2491×

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.

481×

NEEDS ACID

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate acidification.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

831×

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
8/5/2005
16IEE21HERRING, HOT SMOKED, FISH
83NO PROCESS
New York District Office (NYK-DO)
1/10/2003
16AYY21HERRING
62NEEDS FCE
New York District Office (NYK-DO)
1/10/2003
16AYY21HERRING
48NEEDS ACID
New York District Office (NYK-DO)
5/3/2002
16AYE22MACKEREL (ONLY SCOMBEROMORUS SPP EG. SPANISH OR KING)
249FILTHY
482NUTRIT LBL
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Brivais Vilnis's FDA import refusal history?

Brivais Vilnis (FEI: 3002668627) has 4 FDA import refusal record(s) in our database, spanning from 5/3/2002 to 8/5/2005.

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. Brivais Vilnis's FEI number is 3002668627.

What types of violations has Brivais Vilnis received?

Brivais Vilnis has been cited for 5 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 Brivais Vilnis come from?

All FDA import refusal data for Brivais Vilnis 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.