Vinnitsa Confectionery Factory

2 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• LIST INGRE1 refused line

  Ingredients not listed

  The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

• UNSAFE COL1 refused line

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Vinnitsa Confectionery Factory

Is Vinnitsa Confectionery Factory on an FDA import alert?

Yes. As of October 26, 2026, Vinnitsa Confectionery Factory is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for chocolate candy monte cristo w/cherries in cherry liqueur; crazy bee fruity- mixed fruit; gummi candies; FDA published the listing on September 18, 2009.

Has FDA refused shipments from Vinnitsa Confectionery Factory?

Yes. FDA refused 1 shipment line from Vinnitsa Confectionery Factory on August 25, 2017. The most recent, on August 25, 2017, was jellied candy, soft (jelly beans, gum drops, etc.), without nuts and fruit (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Vinnitsa Confectionery Factory's shipments?

The most frequent charges are LIST INGRE (ingredients not listed, 1 line) and UNSAFE COL (color additive unsafe under section 721, 1 line).

What is Vinnitsa Confectionery Factory's FEI number?

Vinnitsa Confectionery Factory's FDA Establishment Identifier (FEI) is 3013174288.

Can shipments from Vinnitsa Confectionery Factory still enter the U.S.?

Shipments of chocolate candy monte cristo w/cherries in cherry liqueur; crazy bee fruity- mixed fruit; gummi candies from Vinnitsa Confectionery 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).