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Vignir G. Jonsson HF

⚠️ Moderate Risk

FEI: 3004343165 • Akranesi, IS-3 • ICELAND

FEI

FEI Number

3004343165

📍

Location

Akranesi, IS-3

🇮🇸

Country

ICELAND
🏢

Address

Smidjuvellir 4, , Akranesi, IS-3, Iceland

Moderate Risk

FDA Import Risk Assessment

38.4
LowModerateHighCritical

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

Statistics

7
Total Refusals
3
Unique Violations
12/2/2005
Latest Refusal
12/2/2005
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

2187×

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.

4827×

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.

837×

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
12/2/2005
16YCO01CAVIAR, FISHERY PRODUCTS, N.E.C.
218LIST INGRE
482NUTRIT LBL
83NO PROCESS
Baltimore District Office (BLT-DO)
12/2/2005
16YCO01CAVIAR, FISHERY PRODUCTS, N.E.C.
218LIST INGRE
482NUTRIT LBL
83NO PROCESS
Baltimore District Office (BLT-DO)
12/2/2005
16YCO01CAVIAR, FISHERY PRODUCTS, N.E.C.
218LIST INGRE
482NUTRIT LBL
83NO PROCESS
Baltimore District Office (BLT-DO)
12/2/2005
16YCO01CAVIAR, FISHERY PRODUCTS, N.E.C.
218LIST INGRE
482NUTRIT LBL
83NO PROCESS
Baltimore District Office (BLT-DO)
12/2/2005
16YCO01CAVIAR, FISHERY PRODUCTS, N.E.C.
218LIST INGRE
482NUTRIT LBL
83NO PROCESS
Baltimore District Office (BLT-DO)
12/2/2005
16YCO01CAVIAR, FISHERY PRODUCTS, N.E.C.
218LIST INGRE
482NUTRIT LBL
83NO PROCESS
Baltimore District Office (BLT-DO)
12/2/2005
16YCO01CAVIAR, FISHERY PRODUCTS, N.E.C.
218LIST INGRE
482NUTRIT LBL
83NO PROCESS
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Vignir G. Jonsson HF's FDA import refusal history?

Vignir G. Jonsson HF (FEI: 3004343165) has 7 FDA import refusal record(s) in our database, spanning from 12/2/2005 to 12/2/2005.

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. Vignir G. Jonsson HF's FEI number is 3004343165.

What types of violations has Vignir G. Jonsson HF received?

Vignir G. Jonsson HF has been cited for 3 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 Vignir G. Jonsson HF come from?

All FDA import refusal data for Vignir G. Jonsson HF 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.