Aviko B.V.
⚠️ Moderate Risk
FEI: 3011392459 • Steenderen, Gelderland • NETHERLANDS
FEI Number
3011392459
Location
Steenderen, Gelderland
Country
NETHERLANDSAddress
Dr. Alfons Ariensstraat 28, , Steenderen, Gelderland, Netherlands
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
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/21/2019 | 24GGT12JALAPENO PEPPER, HOT, BREADED | 473LABELING | Division of Southeast Imports (DSEI) |
| 2/21/2019 | 07SFT02POTATO STARCH SNACKS, BAKED | 328USUAL NAME | Division of Southeast Imports (DSEI) |
| 2/21/2019 | 07QGT05ONION SNACK (FLAVORED OR UNFLAVORED), VEGETABLE SNACKS (OTHER THAN PULSES) BAKED | 328USUAL NAME | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Aviko B.V.'s FDA import refusal history?
Aviko B.V. (FEI: 3011392459) has 3 FDA import refusal record(s) in our database, spanning from 2/21/2019 to 2/21/2019.
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. Aviko B.V.'s FEI number is 3011392459.
What types of violations has Aviko B.V. received?
Aviko B.V. has been cited for 2 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 Aviko B.V. come from?
All FDA import refusal data for Aviko B.V. 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.