Baklawa Made Better Sugar Candies Manufacturing LLC

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

Refusal charges, in plain English

• 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 Baklawa Made Better Sugar Candies Manufacturing LLC

Is Baklawa Made Better Sugar Candies Manufacturing LLC on an FDA import alert?

Yes. As of October 26, 2026, Baklawa Made Better Sugar Candies Manufacturing LLC is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for malban & nougat; FDA published the listing on August 9, 2017.

Has FDA refused shipments from Baklawa Made Better Sugar Candies Manufacturing LLC?

Yes. FDA refused 1 shipment line from Baklawa Made Better Sugar Candies Manufacturing LLC on October 12, 2017. The most recent, on October 12, 2017, was soft candy with nuts or nut products, n.e.c. (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Baklawa Made Better Sugar Candies Manufacturing LLC's shipments?

The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).

When was Baklawa Made Better Sugar Candies Manufacturing LLC last inspected by FDA?

FDA's most recent inspection of Baklawa Made Better Sugar Candies Manufacturing LLC with a final classification is dated February 28, 2019 and was classified VAI (Voluntary Action Indicated).

What is Baklawa Made Better Sugar Candies Manufacturing LLC's FEI number?

Baklawa Made Better Sugar Candies Manufacturing LLC's FDA Establishment Identifier (FEI) is 3011253791.

Can shipments from Baklawa Made Better Sugar Candies Manufacturing LLC still enter the U.S.?

Shipments of malban & nougat from Baklawa Made Better Sugar Candies Manufacturing LLC 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).