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Global Maharaja Pte Ltd

FDA import alert and refusal historyRangoon, MyanmarFEI 3003802486

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Example subjectGlobal Maharaja Pte Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Global Maharaja Pte Ltd (Rangoon, Myanmar) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for freshwater non-ictalurus fish; fish, n.e.c., published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Global Maharaja Pte Ltd

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

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listFreshwater Non-Ictalurus Fish; Fish, N.E.C.
    Source

Questions about Global Maharaja Pte Ltd

Is Global Maharaja Pte Ltd on an FDA import alert?
Yes. As of October 26, 2026, Global Maharaja Pte Ltd is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for freshwater non-ictalurus fish; fish, n.e.c.; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Global Maharaja Pte Ltd?
No FDA import refusals for Global Maharaja Pte Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Global Maharaja Pte Ltd's FEI number?
Global Maharaja Pte Ltd's FDA Establishment Identifier (FEI) is 3003802486.
Can shipments from Global Maharaja Pte Ltd still enter the U.S.?
Shipments of freshwater non-ictalurus fish; fish, n.e.c. from Global Maharaja Pte Ltd can be detained without physical examination under Import Alert 16-81; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectGlobal Maharaja Pte 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.