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Arilje Svetolika Lazarevica

FDA import alert and refusal historyGora, SerbiaFEI 3004146233

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Example subjectArilje Svetolika Lazarevic added to Import Alert 16-129 (red list)

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As of October 26, 2026, Arilje Svetolika Lazarevica (Gora, Serbia) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for 4-berry mix; frozen, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Arilje Svetolika Lazarevica

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 99-08red list4-berry mix; frozen
    Source

Questions about Arilje Svetolika Lazarevica

Is Arilje Svetolika Lazarevica on an FDA import alert?
Yes. As of October 26, 2026, Arilje Svetolika Lazarevica is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for 4-berry mix; frozen; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Arilje Svetolika Lazarevica?
No FDA import refusals for Arilje Svetolika Lazarevica appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Arilje Svetolika Lazarevica's FEI number?
Arilje Svetolika Lazarevica's FDA Establishment Identifier (FEI) is 3004146233.
Can shipments from Arilje Svetolika Lazarevica still enter the U.S.?
Shipments of 4-berry mix; frozen from Arilje Svetolika Lazarevica can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectArilje Svetolika Lazarevic 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.