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Southern Canning Pty Ltd

FDA import alert and refusal historyPortland, AustraliaFEI 3007280260

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Example subjectSouthern Canning Pty Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Southern Canning Pty Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 26, 2026, most often for no scheduled process filed (NO PROCESS).

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

Current status

Import alerts
Not listed
Last import refusal
Abalone · NO PROCESS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Southern Canning Pty Ltd

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

2026

  1. Import refusal
    Refused, AbaloneNO PROCESSEntry EPM-0195535-6
    Source

Refusal charges, in plain English

  • NO PROCESS1 refused line

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Southern Canning Pty Ltd

Is Southern Canning Pty Ltd on an FDA import alert?
No listing for Southern Canning Pty Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Australia page.
Has FDA refused shipments from Southern Canning Pty Ltd?
Yes. FDA refused 1 shipment line from Southern Canning Pty Ltd on August 26, 2026. The most recent, on August 26, 2026, was abalone, charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Southern Canning Pty Ltd's shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
What is Southern Canning Pty Ltd's FEI number?
Southern Canning Pty Ltd's FDA Establishment Identifier (FEI) is 3007280260.

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Example subjectSouthern Canning Pty Lt 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.