PT. Anping Seafood Indonesia
FDA import alert and refusal historyBitung, IndonesiaFEI 3016588182
As of October 26, 2026, PT. Anping Seafood Indonesia (Bitung, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tuna, published by FDA on June 12, 2024, and has 13 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-81 · red list
- Last import refusal
- Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for PT. Anping Seafood Indonesia
15 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0098548-1Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0097552-4Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0096982-4Source
- Import alert listingListed on Import Alert 16-81red listTunaSource
- Import refusalSource
Refused, 2 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 802-0095853-8Show 2 linesHide lines
- Import refusalSource
Refused, 5 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 802-0096606-9Show 5 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 802-0096606-9Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 802-0096606-9Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 802-0096606-9Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 802-0096606-9Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 802-0096606-9Source
- Import refusalSource
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 802-0095853-8Show 3 linesHide lines
2023
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- FILTHY5 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.
- SALMONELLA3 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. Anping Seafood Indonesia
- Is PT. Anping Seafood Indonesia on an FDA import alert?
- Yes. As of October 26, 2026, PT. Anping Seafood Indonesia is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tuna; FDA published the listing on June 12, 2024.
- Has FDA refused shipments from PT. Anping Seafood Indonesia?
- Yes. FDA refused 13 shipment lines from PT. Anping Seafood Indonesia between April 8, 2024 and August 6, 2024. The most recent, on August 6, 2024, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as SALMONELLA (salmonella).
- Why did FDA refuse PT. Anping Seafood Indonesia's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 5 lines) and HISTAMINE (histamine, 5 lines).
- When was PT. Anping Seafood Indonesia last inspected by FDA?
- FDA's most recent inspection of PT. Anping Seafood Indonesia with a final classification is dated January 26, 2023 and was classified VAI (Voluntary Action Indicated).
- What is PT. Anping Seafood Indonesia's FEI number?
- PT. Anping Seafood Indonesia's FDA Establishment Identifier (FEI) is 3016588182.
- Can shipments from PT. Anping Seafood Indonesia still enter the U.S.?
- Shipments of tuna from PT. Anping Seafood Indonesia can be detained without physical examination under Import Alert 16-81; 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.