Icelandic Freezing Plants Corp
⚠️ Moderate Risk
FEI: 1000344805 • Reykjavik • ICELAND
FEI Number
1000344805
Location
Reykjavik
Country
ICELANDAddress
Aoal 6, Box 1525, Reykjavik, , 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
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
Refusal History
Frequently Asked Questions
What is Icelandic Freezing Plants Corp's FDA import refusal history?
Icelandic Freezing Plants Corp (FEI: 1000344805) has 2 FDA import refusal record(s) in our database, spanning from 11/21/2001 to 8/29/2002.
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. Icelandic Freezing Plants Corp's FEI number is 1000344805.
What types of violations has Icelandic Freezing Plants Corp received?
Icelandic Freezing Plants Corp 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 Icelandic Freezing Plants Corp come from?
All FDA import refusal data for Icelandic Freezing Plants Corp 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.