Kk Shinkan
FDA import alert and refusal historyKobe City, JapanFEI 1000488370
As of October 26, 2026, Kk Shinkan (Kobe City, Japan) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for dried radish sengiri daikon, published by FDA on December 18, 2013, 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 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kk Shinkan
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 99-21red listDried Radish Sengiri DaikonSource
Questions about Kk Shinkan
- Is Kk Shinkan on an FDA import alert?
- Yes. As of October 26, 2026, Kk Shinkan is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for dried radish sengiri daikon; FDA published the listing on December 18, 2013.
- Has FDA refused shipments from Kk Shinkan?
- No FDA import refusals for Kk Shinkan appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kk Shinkan's FEI number?
- Kk Shinkan's FDA Establishment Identifier (FEI) is 1000488370.
- Can shipments from Kk Shinkan still enter the U.S.?
- Shipments of dried radish sengiri daikon from Kk Shinkan can be detained without physical examination under Import Alert 99-21; 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.