Gia Don Cookies Enterprises
FDA import alert and refusal historyHo Chi Minh, VietnamFEI 3012985259
Recorded by FDA as GIA DON COOKIES ENTERPRISES
As of October 26, 2026, Gia Don Cookies Enterprises (Ho Chi Minh, Vietnam) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mixed flavor creatus cookie; mixed plain cookies,biscuits and wafers; plain cookies,biscuits and wafers, n.e.c., 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 Gia Don Cookies Enterprises
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listMixed flavor creatus cookie; Mixed Plain Cookies,Biscuits and Wafers; Plain Cookies,Biscuits and Wafers, N.E.C.Source
Questions about Gia Don Cookies Enterprises
- Is Gia Don Cookies Enterprises on an FDA import alert?
- Yes. As of October 26, 2026, Gia Don Cookies Enterprises is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mixed flavor creatus cookie; mixed plain cookies,biscuits and wafers; plain cookies,biscuits and wafers, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Gia Don Cookies Enterprises?
- No FDA import refusals for Gia Don Cookies Enterprises appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Gia Don Cookies Enterprises's FEI number?
- Gia Don Cookies Enterprises's FDA Establishment Identifier (FEI) is 3012985259.
- Can shipments from Gia Don Cookies Enterprises still enter the U.S.?
- Shipments of mixed flavor creatus cookie; mixed plain cookies,biscuits and wafers; plain cookies,biscuits and wafers, n.e.c. from Gia Don Cookies Enterprises 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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