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Simo

FDA import alert and refusal historySarno, ItalyFEI 3013268692

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Example subjectSim added to Import Alert 16-129 (red list)

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As of October 25, 2026, Simo is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 9, 2018, 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
Oil stock olives, olive pomace · USUAL NAME
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Simo

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

2019

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2018

  1. Import refusal
    Refused, Oil stock olives, olive pomaceUSUAL NAMEEntry 300-5470255-0
    Source

Refusal charges, in plain English

  • USUAL NAME1 refused line

    Common or usual name missing

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

Questions about Simo

Is Simo on an FDA import alert?
No listing for Simo appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Italy page.
Has FDA refused shipments from Simo?
Yes. FDA refused 1 shipment line from Simo on July 9, 2018. The most recent, on July 9, 2018, was oil stock olives, olive pomace, charged as USUAL NAME (common or usual name missing).
Why did FDA refuse Simo's shipments?
The most frequent charge is USUAL NAME (common or usual name missing, 1 line).
When was Simo last inspected by FDA?
FDA's most recent inspection of Simo with a final classification is dated February 18, 2019 and was classified NAI (No Action Indicated).
What is Simo's FEI number?
Simo's FDA Establishment Identifier (FEI) is 3013268692.

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Example subjectSim 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.