Agustson Ehf
⚠️ Moderate Risk
FEI: 3005794422 • Stykkisholmi • ICELAND
FEI Number
3005794422
Location
Stykkisholmi
Country
ICELANDAddress
Adalgata 1, , Stykkisholmi, , Iceland
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/22/2018 | 16EGD05SCALLOPS | 249FILTHY | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is Agustson Ehf's FDA import refusal history?
Agustson Ehf (FEI: 3005794422) has 1 FDA import refusal record(s) in our database, spanning from 1/22/2018 to 1/22/2018.
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. Agustson Ehf's FEI number is 3005794422.
What types of violations has Agustson Ehf received?
Agustson Ehf 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 Agustson Ehf come from?
All FDA import refusal data for Agustson Ehf 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.