Vesteralens Hermetikkfabrikk
⚠️ Moderate Risk
FEI: 1000196557 • Sortnand • 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
UNDER PRC
The article appears to have inadequate processing in having been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
Frequently Asked Questions
What is Vesteralens Hermetikkfabrikk's FDA import refusal history?
Vesteralens Hermetikkfabrikk (FEI: 1000196557) has 2 FDA import refusal record(s) in our database, spanning from 2/14/2002 to 2/14/2002.
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. Vesteralens Hermetikkfabrikk's FEI number is 1000196557.
What types of violations has Vesteralens Hermetikkfabrikk received?
Vesteralens Hermetikkfabrikk 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 Vesteralens Hermetikkfabrikk come from?
All FDA import refusal data for Vesteralens Hermetikkfabrikk 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.