International Gift Gallery Factory
FDA import alert and refusal historyShenzhen, ChinaFEI 3003529606
As of October 26, 2026, International Gift Gallery Factory (Shenzhen, China) 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), 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 International Gift Gallery Factory
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)Source
Questions about International Gift Gallery Factory
- Is International Gift Gallery Factory on an FDA import alert?
- Yes. As of October 26, 2026, International Gift Gallery Factory 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); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from International Gift Gallery Factory?
- No FDA import refusals for International Gift Gallery Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is International Gift Gallery Factory's FEI number?
- International Gift Gallery Factory's FDA Establishment Identifier (FEI) is 3003529606.
- Can shipments from International Gift Gallery Factory still enter the U.S.?
- Shipments of candy bar or pieces (not caramel or fondant), hard, without nuts and fruit (without chocolate) from International Gift Gallery 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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