Shimadi Keijo Shoten Ltd
FDA import alert and refusal historyTochigi, JapanFEI 12397
As of October 26, 2026, Shimadi Keijo Shoten Ltd (Tochigi, Japan) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for gourd, dried or paste, published by FDA on September 16, 2009, 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 Shimadi Keijo Shoten Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-21red listGourd, Dried or PasteSource
Questions about Shimadi Keijo Shoten Ltd
- Is Shimadi Keijo Shoten Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Shimadi Keijo Shoten Ltd is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for gourd, dried or paste; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Shimadi Keijo Shoten Ltd?
- No FDA import refusals for Shimadi Keijo Shoten Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Shimadi Keijo Shoten Ltd's FEI number?
- Shimadi Keijo Shoten Ltd's FDA Establishment Identifier (FEI) is 12397.
- Can shipments from Shimadi Keijo Shoten Ltd still enter the U.S.?
- Shipments of gourd, dried or paste from Shimadi Keijo Shoten Ltd 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.