PT Trijaya Megah
FDA import alert and refusal historyTangerang, IndonesiaFEI 3010137826
As of October 26, 2026, PT Trijaya Megah (Tangerang, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for dried salted jeprox fish fillet; sole, published by FDA on December 7, 2017, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-81 · red list
- Last import refusal
- Fish, n.e.c. · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for PT Trijaya Megah
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Fish, n.e.c.SALMONELLAEntry FS2-1166233-3Source
- Import alert listingListed on Import Alert 16-81red listDried Salted Jeprox Fish Fillet; SoleSource
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about PT Trijaya Megah
- Is PT Trijaya Megah on an FDA import alert?
- Yes. As of October 26, 2026, PT Trijaya Megah is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for dried salted jeprox fish fillet; sole; FDA published the listing on December 7, 2017.
- Has FDA refused shipments from PT Trijaya Megah?
- Yes. FDA refused 1 shipment line from PT Trijaya Megah on December 21, 2017. The most recent, on December 21, 2017, was fish, n.e.c., charged as SALMONELLA (salmonella).
- Why did FDA refuse PT Trijaya Megah's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is PT Trijaya Megah's FEI number?
- PT Trijaya Megah's FDA Establishment Identifier (FEI) is 3010137826.
- Can shipments from PT Trijaya Megah still enter the U.S.?
- Shipments of dried salted jeprox fish fillet; sole from PT Trijaya Megah 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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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.