Kwang Confectionery Company
FDA import alert and refusal historyPusan, South KoreaFEI 3001744174
As of October 26, 2026, Kwang Confectionery Company (Pusan, South Korea) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for candy bar or pieces (not caramel or fondant), hard, without nuts and fruit (without chocolate); nuroonggi candy, published by FDA on September 18, 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 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 Kwang Confectionery Company
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listCandy Bar or Pieces (not Caramel or Fondant), Hard, without Nuts and Fruit (without Chocolate); nuroonggi candySource
Questions about Kwang Confectionery Company
- Is Kwang Confectionery Company on an FDA import alert?
- Yes. As of October 26, 2026, Kwang Confectionery Company is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for candy bar or pieces (not caramel or fondant), hard, without nuts and fruit (without chocolate); nuroonggi candy; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Kwang Confectionery Company?
- No FDA import refusals for Kwang Confectionery Company appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kwang Confectionery Company's FEI number?
- Kwang Confectionery Company's FDA Establishment Identifier (FEI) is 3001744174.
- Can shipments from Kwang Confectionery Company still enter the U.S.?
- Shipments of candy bar or pieces (not caramel or fondant), hard, without nuts and fruit (without chocolate); nuroonggi candy from Kwang Confectionery Company 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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