Has FDA refused shipments from PT. Anugrah Laut Indonesia?

Yes. FDA refused 18 shipment lines from PT. Anugrah Laut Indonesia between June 15, 2023 and January 6, 2025. The most recent, on January 6, 2025, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as HISTAMINE (histamine).

Why did FDA refuse PT. Anugrah Laut Indonesia's shipments?

The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 13 lines) and HISTAMINE (histamine, 5 lines).

When was PT. Anugrah Laut Indonesia last inspected by FDA?

FDA's most recent inspection of PT. Anugrah Laut Indonesia with a final classification is dated December 5, 2024 and was classified OAI (Official Action Indicated).

What is PT. Anugrah Laut Indonesia's FEI number?

PT. Anugrah Laut Indonesia's FDA Establishment Identifier (FEI) is 3020093558.

Can shipments from PT. Anugrah Laut Indonesia still enter the U.S.?

Shipments of vacuum-packed tuna from PT. Anugrah Laut Indonesia can be detained without physical examination under Import Alert 16-120; 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).

PT. Anugrah Laut Indonesia

FDA import alert and refusal historyTuban, IndonesiaFEI 3020093558

Watch this supplier

As of October 26, 2026, PT. Anugrah Laut Indonesia (Tuban, Indonesia) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for vacuum-packed tuna, published by FDA on May 23, 2025, and has 18 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: IA 16-120 · red list
Last import refusal: Jan 6, 2025Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · HISTAMINE
Last warning letter: None found
Last inspection: Dec 5, 2024Classified OAI (Official Action Indicated)

Every FDA record for PT. Anugrah Laut Indonesia

20 records, newest first. Each line links to the FDA page it came from.

2025

May 23, 2025Import alert listing
Listed on Import Alert 16-120red listVacuum-packed Tuna
Source
Jan 6, 2025Import refusal
Refused, 5 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 082-0454707-2Show 5 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 082-0454707-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 082-0454707-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 082-0454707-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 082-0454707-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 082-0454707-2Source
Source

2024

Dec 5, 2024Inspection
Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
Source
Apr 11, 2024Import refusal
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0158240-6Show 3 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0158240-6Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0158240-6Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0158240-6Source
Source

2023

Dec 28, 2023Import refusal
Refused, Shrimp & prawnsFILTHY SALMONELLAEntry B5D-0011539-7
Source
Jun 15, 2023Import refusal
Refused, 9 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Show 9 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry AMG-0153730-1Source
Source

Refusal charges, in plain English

FILTHY13 refused lines
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.
HISTAMINE5 refused lines
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
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. Anugrah Laut Indonesia

Is PT. Anugrah Laut Indonesia on an FDA import alert?: Yes. As of October 26, 2026, PT. Anugrah Laut Indonesia is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for vacuum-packed tuna; FDA published the listing on May 23, 2025.
Has FDA refused shipments from PT. Anugrah Laut Indonesia?: Yes. FDA refused 18 shipment lines from PT. Anugrah Laut Indonesia between June 15, 2023 and January 6, 2025. The most recent, on January 6, 2025, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as HISTAMINE (histamine).
Why did FDA refuse PT. Anugrah Laut Indonesia's shipments?: The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 13 lines) and HISTAMINE (histamine, 5 lines).
When was PT. Anugrah Laut Indonesia last inspected by FDA?: FDA's most recent inspection of PT. Anugrah Laut Indonesia with a final classification is dated December 5, 2024 and was classified OAI (Official Action Indicated).
What is PT. Anugrah Laut Indonesia's FEI number?: PT. Anugrah Laut Indonesia's FDA Establishment Identifier (FEI) is 3020093558.
Can shipments from PT. Anugrah Laut Indonesia still enter the U.S.?: Shipments of vacuum-packed tuna from PT. Anugrah Laut Indonesia can be detained without physical examination under Import Alert 16-120; 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).

Watch this supplier

Get an email when FDA publishes anything new on PT. Anugrah Laut Indonesia.

An email with the FDA source, and a dated PDF for your FSVP file. First supplier free.

Watch this supplier

Related records

Similar suppliers in Indonesia

Guides

Get this record's changes by email

Watch this supplier

Buying from PT. Anugrah Laut Indonesia?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

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.