PT. Sig Asia
FDA import alert and refusal historyBitung, IndonesiaFEI 3011457005
Recorded by FDA as PT. SIG ASIA
As of October 25, 2026, PT. Sig Asia (Bitung, Indonesia) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for all fish and fishery products, published by FDA on October 12, 2011, and has 8 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-119 · red list
- Last import refusal
- Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for PT. Sig Asia
10 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry ES6-4043608-6Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry K64-1057977-0Source
- Import refusalSource
Refused, 4 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry K64-1056453-3Show 4 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry K64-1056453-3Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry K64-1056453-3Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry K64-1056453-3Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry K64-1056453-3Source
2018
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2017
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYSALMONELLAEntry 109-0946853-9Source
2016
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 98F-0010398-4Source
2011
- Import alert listingListed on Import Alert 16-119red listAll fish and fishery productsSource
Refusal charges, in plain English
- HISTAMINE4 refused lines
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
- 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.
- SALMONELLA2 refused lines
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. Sig Asia
- Is PT. Sig Asia on an FDA import alert?
- Yes. As of October 25, 2026, PT. Sig Asia is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for all fish and fishery products; FDA published the listing on October 12, 2011.
- Has FDA refused shipments from PT. Sig Asia?
- Yes. FDA refused 8 shipment lines from PT. Sig Asia between December 22, 2016 and December 9, 2019. The most recent, on December 9, 2019, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse PT. Sig Asia's shipments?
- The most frequent charges are HISTAMINE (histamine, 4 lines) and FILTHY (filthy, putrid or decomposed substance, 3 lines).
- When was PT. Sig Asia last inspected by FDA?
- FDA's most recent inspection of PT. Sig Asia with a final classification is dated September 18, 2018 and was classified VAI (Voluntary Action Indicated).
- What is PT. Sig Asia's FEI number?
- PT. Sig Asia's FDA Establishment Identifier (FEI) is 3011457005.
- Can shipments from PT. Sig Asia still enter the U.S.?
- Shipments of all fish and fishery products from PT. Sig Asia can be detained without physical examination under Import Alert 16-119; 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.