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Mgs Beverages Co.,Ltd.

FDA import alert and refusal historyYangon, MyanmarFEI 3003526359

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Example subjectMgs Beverages Co.,Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Mgs Beverages Co.,Ltd. (Yangon, 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 Mgs Beverages Co.,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 Mgs Beverages Co.,Ltd.

Is Mgs Beverages Co.,Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Mgs Beverages Co.,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 Mgs Beverages Co.,Ltd.?
No FDA import refusals for Mgs Beverages Co.,Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Mgs Beverages Co.,Ltd.'s FEI number?
Mgs Beverages Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3003526359.
Can shipments from Mgs Beverages Co.,Ltd. still enter the U.S.?
Shipments of freshwater non-ictalurus fish; fish, n.e.c. from Mgs Beverages Co.,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 subjectMgs Beverages Co.,Ltd 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.