PT. Shikamase Lakasana Cipta
FDA import alert and refusal historyBekasi, IndonesiaFEI 3012065950
Recorded by FDA as PT. SHIKAMASE LAKASANA CIPTA
As of October 26, 2026, PT. Shikamase Lakasana Cipta (Bekasi, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tuna, published by FDA on December 21, 2017, and has 3 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.) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for PT. Shikamase Lakasana Cipta
4 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry KM6-3509620-9Show 3 linesHide lines
- Import alert listingListed on Import Alert 16-81red listTunaSource
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. Shikamase Lakasana Cipta
- Is PT. Shikamase Lakasana Cipta on an FDA import alert?
- Yes. As of October 26, 2026, PT. Shikamase Lakasana Cipta is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tuna; FDA published the listing on December 21, 2017.
- Has FDA refused shipments from PT. Shikamase Lakasana Cipta?
- Yes. FDA refused 3 shipment lines from PT. Shikamase Lakasana Cipta on December 29, 2017. The most recent, on December 29, 2017, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse PT. Shikamase Lakasana Cipta's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
- What is PT. Shikamase Lakasana Cipta's FEI number?
- PT. Shikamase Lakasana Cipta's FDA Establishment Identifier (FEI) is 3012065950.
- Can shipments from PT. Shikamase Lakasana Cipta still enter the U.S.?
- Shipments of tuna from PT. Shikamase Lakasana Cipta 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.