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Aviko B.V.

FDA import alert and refusal historySteenderen, NetherlandsFEI 3011392459

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Example subjectAviko B.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Aviko B.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on February 21, 2019, most often for common or usual name missing (USUAL NAME).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Jalapeno pepper, hot, breaded · LABELING
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Aviko B.V.

4 records, newest first. Each line links to the FDA page it came from.

2019

  1. Import refusal
    Refused, 3 lines in one entry: Jalapeno pepper, hot, breaded; Potato starch snacks, baked and 1 moreLABELINGUSUAL NAMEEntry 261-0537403-2Show 3 lines
    • Refused, Jalapeno pepper, hot, breadedLABELINGEntry 261-0537403-2Source
    • Refused, Potato starch snacks, bakedUSUAL NAMEEntry 261-0537403-2Source
    • Refused, Onion snack (flavored or unflavored), vegetable snacks (other than pulses) bakedUSUAL NAMEEntry 261-0537403-2Source
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • USUAL NAME2 refused lines

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

Questions about Aviko B.V.

Is Aviko B.V. on an FDA import alert?
No listing for Aviko B.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
Has FDA refused shipments from Aviko B.V.?
Yes. FDA refused 3 shipment lines from Aviko B.V. on February 21, 2019. The most recent, on February 21, 2019, was jalapeno pepper, hot, breaded, charged as LABELING (fair packaging and labeling act).
Why did FDA refuse Aviko B.V.'s shipments?
The most frequent charges are USUAL NAME (common or usual name missing, 2 lines) and LABELING (fair packaging and labeling act, 1 line).
When was Aviko B.V. last inspected by FDA?
FDA's most recent inspection of Aviko B.V. with a final classification is dated March 14, 2018 and was classified VAI (Voluntary Action Indicated).
What is Aviko B.V.'s FEI number?
Aviko B.V.'s FDA Establishment Identifier (FEI) is 3011392459.

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Example subjectAviko B.V added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.