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Arcor Saic

FDA import alert and refusal historyVilla Mercedes, ArgentinaFEI 3004383016

Recorded by FDA as ARCOR SAIC

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

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As of October 25, 2026, Arcor Saic is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 28, 2023, most often for salmonella (SALMONELLA).

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

Current status

Import alerts
Not listed
Last import refusal
Creme filled/iced cookie,biscuit,wafer · SALMONELLA
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Arcor Saic

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

2023

  1. Import refusal
    Refused, Creme filled/iced cookie,biscuit,waferSALMONELLAEntry 739-6314612-8
    Source

2019

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2011

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

2009

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • SALMONELLA1 refused line

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Arcor Saic

Is Arcor Saic on an FDA import alert?
No listing for Arcor Saic appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Argentina page.
Has FDA refused shipments from Arcor Saic?
Yes. FDA refused 1 shipment line from Arcor Saic on August 28, 2023. The most recent, on August 28, 2023, was creme filled/iced cookie,biscuit,wafer, charged as SALMONELLA (salmonella).
Why did FDA refuse Arcor Saic's shipments?
The most frequent charge is SALMONELLA (salmonella, 1 line).
When was Arcor Saic last inspected by FDA?
FDA's most recent inspection of Arcor Saic with a final classification is dated May 9, 2019 and was classified NAI (No Action Indicated).
What is Arcor Saic's FEI number?
Arcor Saic's FDA Establishment Identifier (FEI) is 3004383016.

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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.