Oao Confectionary Factory Kuban
FDA import alert and refusal historyTimashevsk, RussiaFEI 3003843057
As of October 26, 2026, Oao Confectionary Factory Kuban (Timashevsk, Russia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mixed plain cookies,biscuits and wafers; fruit/fruit flavored plain cookies, biscuits and wafers, 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 Oao Confectionary Factory Kuban
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listMixed Plain Cookies,Biscuits and Wafers; Fruit/Fruit Flavored Plain Cookies, Biscuits and WafersSource
Questions about Oao Confectionary Factory Kuban
- Is Oao Confectionary Factory Kuban on an FDA import alert?
- Yes. As of October 26, 2026, Oao Confectionary Factory Kuban is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mixed plain cookies,biscuits and wafers; fruit/fruit flavored plain cookies, biscuits and wafers; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Oao Confectionary Factory Kuban?
- No FDA import refusals for Oao Confectionary Factory Kuban appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Oao Confectionary Factory Kuban's FEI number?
- Oao Confectionary Factory Kuban's FDA Establishment Identifier (FEI) is 3003843057.
- Can shipments from Oao Confectionary Factory Kuban still enter the U.S.?
- Shipments of mixed plain cookies,biscuits and wafers; fruit/fruit flavored plain cookies, biscuits and wafers from Oao Confectionary Factory Kuban 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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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.