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PT. Intra Niaga Mulya

FDA import alert and refusal historyBandar Lampung, IndonesiaFEI 3037138917

Recorded by FDA as PT. INTRA NIAGA MULYA

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Example subjectPT. Intra Niaga Muly added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Intra Niaga Mulya is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 3, 2026, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Coffee, beans · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for PT. Intra Niaga Mulya

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

2026

  1. Import refusal
    Refused, Coffee, beansFILTHYEntry 238-2026094-3
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about PT. Intra Niaga Mulya

Is PT. Intra Niaga Mulya on an FDA import alert?
No listing for PT. Intra Niaga Mulya appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
Has FDA refused shipments from PT. Intra Niaga Mulya?
Yes. FDA refused 1 shipment line from PT. Intra Niaga Mulya on June 3, 2026. The most recent, on June 3, 2026, was coffee, beans, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse PT. Intra Niaga Mulya's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is PT. Intra Niaga Mulya's FEI number?
PT. Intra Niaga Mulya's FDA Establishment Identifier (FEI) is 3037138917.

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Example subjectPT. Intra Niaga Muly 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.