Yassine Delight Factory

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

Refusal charges, in plain English

• PESTICIDE5 refused lines

  Pesticide chemical residue

  The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

• FILTHY1 refused line

  Filthy, putrid or decomposed substance

  The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Yassine Delight Factory

Is Yassine Delight Factory on an FDA import alert?

Yes. As of October 26, 2026, Yassine Delight Factory is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for dates; FDA published the listing on May 2, 2024.

Has FDA refused shipments from Yassine Delight Factory?

Yes. FDA refused 6 shipment lines from Yassine Delight Factory between July 6, 2022 and November 13, 2024. The most recent, on November 13, 2024, was dates, dried or paste, charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse Yassine Delight Factory's shipments?

The most frequent charges are PESTICIDE (pesticide chemical residue, 5 lines) and FILTHY (filthy, putrid or decomposed substance, 1 line).

When was Yassine Delight Factory last inspected by FDA?

FDA's most recent inspection of Yassine Delight Factory with a final classification is dated June 16, 2023 and was classified NAI (No Action Indicated).

What is Yassine Delight Factory's FEI number?

Yassine Delight Factory's FDA Establishment Identifier (FEI) is 3006474982.

Can shipments from Yassine Delight Factory still enter the U.S.?

Shipments of dates from Yassine Delight Factory can be detained without physical examination under Import Alert 99-08; 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).