PT Aneka Tuna Indonesia
FDA import alert and refusal historyPasuruan, IndonesiaFEI 3015283272
As of October 26, 2026, PT Aneka Tuna Indonesia is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 11, 2018, 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
- Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for PT Aneka Tuna Indonesia
3 records, newest first. Each line links to the FDA page it came from.
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 Aneka Tuna Indonesia
- Is PT Aneka Tuna Indonesia on an FDA import alert?
- No listing for PT Aneka Tuna Indonesia 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 Aneka Tuna Indonesia?
- Yes. FDA refused 1 shipment line from PT Aneka Tuna Indonesia on June 11, 2018. The most recent, on June 11, 2018, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse PT Aneka Tuna Indonesia's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was PT Aneka Tuna Indonesia last inspected by FDA?
- FDA's most recent inspection of PT Aneka Tuna Indonesia with a final classification is dated November 14, 2022 and was classified NAI (No Action Indicated).
- What is PT Aneka Tuna Indonesia's FEI number?
- PT Aneka Tuna Indonesia's FDA Establishment Identifier (FEI) is 3015283272.
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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.