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FMF Snax Pte Limited

FDA import alert and refusal historySuva, FijiFEI 3006041323

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Example subjectFMF Snax Pte Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, FMF Snax Pte Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 7, 2017, most often for ingredients not listed (LIST INGRE).

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

Current status

Import alerts
Not listed
Last import refusal
Noodles and noodle products, n.e.c. · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for FMF Snax Pte Limited

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

2017

  1. Import refusal
    Refused, 2 lines in one entry: Noodles and noodle products, n.e.c.LIST INGREEntry 9MU-2642881-2Show 2 lines
    Source

Refusal charges, in plain English

  • LIST INGRE2 refused lines

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

Questions about FMF Snax Pte Limited

Is FMF Snax Pte Limited on an FDA import alert?
No listing for FMF Snax Pte Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Fiji page.
Has FDA refused shipments from FMF Snax Pte Limited?
Yes. FDA refused 2 shipment lines from FMF Snax Pte Limited on November 7, 2017. The most recent, on November 7, 2017, was noodles and noodle products, n.e.c., charged as LIST INGRE (ingredients not listed).
Why did FDA refuse FMF Snax Pte Limited's shipments?
The most frequent charge is LIST INGRE (ingredients not listed, 2 lines).
What is FMF Snax Pte Limited's FEI number?
FMF Snax Pte Limited's FDA Establishment Identifier (FEI) is 3006041323.

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Example subjectFMF Snax Pte Limite 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.