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PT. Mega Pratama Indo

FDA import alert and refusal historyKawasan Industri Makassar, IndonesiaFEI 3005280606

Recorded by FDA as PT. MEGA PRATAMA INDO

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Example subjectPT. Mega Pratama Ind added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Mega Pratama Indo (Kawasan Industri Makassar, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tuna, published by FDA on September 30, 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 PT. Mega Pratama Indo

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 listTuna
    Source

Questions about PT. Mega Pratama Indo

Is PT. Mega Pratama Indo on an FDA import alert?
Yes. As of October 26, 2026, PT. Mega Pratama Indo is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tuna; FDA published the listing on September 30, 2009.
Has FDA refused shipments from PT. Mega Pratama Indo?
No FDA import refusals for PT. Mega Pratama Indo appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is PT. Mega Pratama Indo's FEI number?
PT. Mega Pratama Indo's FDA Establishment Identifier (FEI) is 3005280606.
Can shipments from PT. Mega Pratama Indo still enter the U.S.?
Shipments of tuna from PT. Mega Pratama Indo 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 subjectPT. Mega Pratama Ind 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.