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The Maggah Company Limited

FDA import alert and refusal historyKawkayeit, MyanmarFEI 3022476397

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Example subjectThe Maggah Company Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, The Maggah Company Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 22, 2024, most often for poisonous or deleterious substance (POISONOUS).

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

Current status

Import alerts
Not listed
Last import refusal
Betel nut, topping · POISONOUS
Last warning letter
None found
Last inspection
None on record

Every FDA record for The Maggah Company Limited

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

2024

  1. Import refusal
    Refused, Betel nut, toppingPOISONOUSEntry E94-2002770-4
    Source

Refusal charges, in plain English

  • POISONOUS1 refused line

    Poisonous or deleterious substance

    The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

Questions about The Maggah Company Limited

Is The Maggah Company Limited on an FDA import alert?
No listing for The Maggah Company Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Myanmar page.
Has FDA refused shipments from The Maggah Company Limited?
Yes. FDA refused 1 shipment line from The Maggah Company Limited on August 22, 2024. The most recent, on August 22, 2024, was betel nut, topping, charged as POISONOUS (poisonous or deleterious substance).
Why did FDA refuse The Maggah Company Limited's shipments?
The most frequent charge is POISONOUS (poisonous or deleterious substance, 1 line).
What is The Maggah Company Limited's FEI number?
The Maggah Company Limited's FDA Establishment Identifier (FEI) is 3022476397.

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Example subjectThe Maggah Company 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.