SupplierRadar

Muang Mai Mark T

FDA import alert and refusal historyChiang Mai, ThailandFEI 3045812211

Recorded by FDA as MUANG MAI MARK T

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Example subjectMuang Mai Mark added to Import Alert 16-129 (red list)

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As of October 26, 2026, Muang Mai Mark T is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 8, 2026, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Tamarind (subtropical and tropical fruit) · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Muang Mai Mark T

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

2026

  1. Import refusal
    Refused, Tamarind (subtropical and tropical fruit)FILTHYEntry AEK-2080871-2
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Muang Mai Mark T

Is Muang Mai Mark T on an FDA import alert?
No listing for Muang Mai Mark T appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Thailand page.
Has FDA refused shipments from Muang Mai Mark T?
Yes. FDA refused 1 shipment line from Muang Mai Mark T on October 8, 2026. The most recent, on October 8, 2026, was tamarind (subtropical and tropical fruit), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Muang Mai Mark T's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Muang Mai Mark T's FEI number?
Muang Mai Mark T's FDA Establishment Identifier (FEI) is 3045812211.

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Example subjectMuang Mai Mark 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.