Aalesundfisk As
⚠️ Moderate Risk
FEI: 3010089001 • Alesund • NORWAY
FEI Number
3010089001
Location
Alesund
Country
NORWAYAddress
Postboks 2021 Kjopmannsgate 37, , Alesund, , Norway
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
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/10/2014 | 16AHT21HERRING | 308MFR INSAN | Minneapolis District Office (MIN-DO) |
Frequently Asked Questions
What is Aalesundfisk As's FDA import refusal history?
Aalesundfisk As (FEI: 3010089001) has 1 FDA import refusal record(s) in our database, spanning from 12/10/2014 to 12/10/2014.
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. Aalesundfisk As's FEI number is 3010089001.
What types of violations has Aalesundfisk As received?
Aalesundfisk As 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 Aalesundfisk As come from?
All FDA import refusal data for Aalesundfisk As 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.