Minamoto Kitchoan Co Ltd CHIKKO FACTORY
FDA import alert and refusal historyOkayama, JapanFEI 1000168314
As of October 26, 2026, Minamoto Kitchoan Co Ltd CHIKKO FACTORY (Okayama, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mainohana steamed bean cake; bean jelly tsukininishiki; fruit jelly grace dew fruit, published by FDA on March 15, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Minamoto Kitchoan Co Ltd CHIKKO FACTORY
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 45-02red listMainohana Steamed bean cake; Bean Jelly Tsukininishiki; Fruit Jelly Grace Dew FruitSource
Questions about Minamoto Kitchoan Co Ltd CHIKKO FACTORY
- Is Minamoto Kitchoan Co Ltd CHIKKO FACTORY on an FDA import alert?
- Yes. As of October 26, 2026, Minamoto Kitchoan Co Ltd CHIKKO FACTORY is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mainohana steamed bean cake; bean jelly tsukininishiki; fruit jelly grace dew fruit; FDA published the listing on March 15, 2013.
- Has FDA refused shipments from Minamoto Kitchoan Co Ltd CHIKKO FACTORY?
- No FDA import refusals for Minamoto Kitchoan Co Ltd CHIKKO FACTORY appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Minamoto Kitchoan Co Ltd CHIKKO FACTORY's FEI number?
- Minamoto Kitchoan Co Ltd CHIKKO FACTORY's FDA Establishment Identifier (FEI) is 1000168314.
- Can shipments from Minamoto Kitchoan Co Ltd CHIKKO FACTORY still enter the U.S.?
- Shipments of mainohana steamed bean cake; bean jelly tsukininishiki; fruit jelly grace dew fruit from Minamoto Kitchoan Co Ltd CHIKKO FACTORY can be detained without physical examination under Import Alert 45-02; 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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