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VICIUNAI IR PARTNERIAI UAB

⚠️ Moderate Risk

FEI: 3004266435 • Plunge, Telsiu • LITHUANIA

FEI

FEI Number

3004266435

📍

Location

Plunge, Telsiu

🇱🇹

Country

LITHUANIA
🏢

Address

Senamiescio A. 7, , Plunge, Telsiu, Lithuania

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

3
Total Refusals
7
Unique Violations
5/16/2011
Latest Refusal
6/15/2004
Earliest Refusal

Score Breakdown

Violation Severity
66.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
4.3×10%
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

3082×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

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.

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

Refusal History

DateProductViolationsDivision
5/16/2011
16SGT99FISH, COLD SMOKED N.E.C.
308MFR INSAN
New York District Office (NYK-DO)
1/21/2010
16AGT21HERRING
11UNSAFE COL
218LIST INGRE
3300ALLERGEN
3320TRANSFAT
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
6/15/2004
16AHP33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
308MFR INSAN
New York District Office (NYK-DO)

Frequently Asked Questions

What is VICIUNAI IR PARTNERIAI UAB's FDA import refusal history?

VICIUNAI IR PARTNERIAI UAB (FEI: 3004266435) has 3 FDA import refusal record(s) in our database, spanning from 6/15/2004 to 5/16/2011.

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. VICIUNAI IR PARTNERIAI UAB's FEI number is 3004266435.

What types of violations has VICIUNAI IR PARTNERIAI UAB received?

VICIUNAI IR PARTNERIAI UAB has been cited for 7 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 VICIUNAI IR PARTNERIAI UAB come from?

All FDA import refusal data for VICIUNAI IR PARTNERIAI UAB 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.