Sanko Co.,Ltd
FDA import alert and refusal historyAgeo-Shi, JapanFEI 3007377453
As of October 26, 2026, Sanko Co.,Ltd (AGEO-SHI, Japan) is on the red list of FDA Import Alert 45-06 (Stevia leaves, crude extracts and foods containing them) for pickled eggplant (shiba nasu); pickled cucumber (shiso kyuri)/(akashiba ippon), published by FDA on January 22, 2015, is also listed on Import Alert 16-119 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-06 · red listIA 16-119 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sanko Co.,Ltd
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 45-06red listPickled Eggplant (Shiba Nasu); Pickled Cucumber (Shiso Kyuri)/(Akashiba Ippon)Source
2013
- Import alert listingListed on Import Alert 16-119red listSalmon FlakesSource
Questions about Sanko Co.,Ltd
- Is Sanko Co.,Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Sanko Co.,Ltd is on the red list of FDA Import Alert 45-06, “Stevia leaves, crude extracts and foods containing them”, for pickled eggplant (shiba nasu); pickled cucumber (shiso kyuri)/(akashiba ippon); FDA published the listing on January 22, 2015.
- Has FDA refused shipments from Sanko Co.,Ltd?
- No FDA import refusals for Sanko Co.,Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Sanko Co.,Ltd's FEI number?
- Sanko Co.,Ltd's FDA Establishment Identifier (FEI) is 3007377453.
- Can shipments from Sanko Co.,Ltd still enter the U.S.?
- Shipments of pickled eggplant (shiba nasu); pickled cucumber (shiso kyuri)/(akashiba ippon) from Sanko Co.,Ltd can be detained without physical examination under Import Alert 45-06; 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.