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Martin Stoifl

FDA import alert and refusal historyFreidersbach, AustraliaFEI 3013394763

Recorded by FDA as MARTIN STOIFL

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

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As of October 26, 2026, Martin Stoifl is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on April 27, 2017, most often for required label information not in english (NO ENGLISH).

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

Current status

Import alerts
Not listed
Last import refusal
Cereal preparations not elsewhere mentioned, n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Martin Stoifl

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

2017

  1. Import refusal
    Refused, Cereal preparations not elsewhere mentioned, n.e.c.NO ENGLISHEntry AEK-3146192-1
    Source

Refusal charges, in plain English

  • NO ENGLISH1 refused line

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

Questions about Martin Stoifl

Is Martin Stoifl on an FDA import alert?
No listing for Martin Stoifl 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 Martin Stoifl?
Yes. FDA refused 1 shipment line from Martin Stoifl on April 27, 2017. The most recent, on April 27, 2017, was cereal preparations not elsewhere mentioned, n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Martin Stoifl's shipments?
The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
What is Martin Stoifl's FEI number?
Martin Stoifl's FDA Establishment Identifier (FEI) is 3013394763.

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Example subjectMartin Stoif 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.