Is PT. Primo Indo Ikan on an FDA import alert?

Yes. As of October 26, 2026, PT. Primo Indo Ikan is on the green list of FDA Import Alert 16-125, “Refrigerated raw fish in reduced oxygen packaging”, for fresh vacuum packed fish; FDA published the listing on March 24, 2010.

Has FDA refused shipments from PT. Primo Indo Ikan?

Yes. FDA refused 3 shipment lines from PT. Primo Indo Ikan on July 18, 2018. The most recent, on July 18, 2018, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as FILTHY (filthy, putrid or decomposed substance).

Why did FDA refuse PT. Primo Indo Ikan's shipments?

The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).

When was PT. Primo Indo Ikan last inspected by FDA?

FDA's most recent inspection of PT. Primo Indo Ikan with a final classification is dated January 22, 2019 and was classified OAI (Official Action Indicated).

What is PT. Primo Indo Ikan's FEI number?

PT. Primo Indo Ikan's FDA Establishment Identifier (FEI) is 3013359716.

PT. Primo Indo Ikan

FDA import alert and refusal historyDenpasar, IndonesiaFEI 3013359716

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As of October 26, 2026, PT. Primo Indo Ikan is on the green list of FDA Import Alert 16-125, which exempts its listed products from detention without physical examination under that alert, and has 3 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 16-125 · green list
Last import refusal: Jul 18, 2018Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · FILTHY
Last warning letter: None found
Last inspection: Jan 22, 2019Classified OAI (Official Action Indicated)

Every FDA record for PT. Primo Indo Ikan

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

2019

Jan 22, 2019Inspection
Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
Source

2018

Jul 18, 2018Import refusal
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 555-0662792-0Show 3 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 555-0662792-0Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 555-0662792-0Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 555-0662792-0Source
Source

2013

Jun 19, 2013Inspection
Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
Source

2012

Apr 3, 2012Inspection
Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
Source

2010

Mar 24, 2010Import alert listing
Listed on Import Alert 16-125green listFresh Vacuum Packed Fish
Source

Refusal charges, in plain English

FILTHY3 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.

Questions about PT. Primo Indo Ikan

Is PT. Primo Indo Ikan on an FDA import alert?: Yes. As of October 26, 2026, PT. Primo Indo Ikan is on the green list of FDA Import Alert 16-125, “Refrigerated raw fish in reduced oxygen packaging”, for fresh vacuum packed fish; FDA published the listing on March 24, 2010.
Has FDA refused shipments from PT. Primo Indo Ikan?: Yes. FDA refused 3 shipment lines from PT. Primo Indo Ikan on July 18, 2018. The most recent, on July 18, 2018, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse PT. Primo Indo Ikan's shipments?: The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
When was PT. Primo Indo Ikan last inspected by FDA?: FDA's most recent inspection of PT. Primo Indo Ikan with a final classification is dated January 22, 2019 and was classified OAI (Official Action Indicated).
What is PT. Primo Indo Ikan's FEI number?: PT. Primo Indo Ikan's FDA Establishment Identifier (FEI) is 3013359716.

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