Cartier Saada SA

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

Refusal charges, in plain English

• NUTRIT LBL6 refused lines

  Nutrition information missing from label

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

• NO PROCESS5 refused lines

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

• LABELING3 refused lines

  Fair Packaging and Labeling Act

  The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

• LACKS FIRM1 refused line

  Manufacturer name and address missing

  The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

• LACKS N/C1 refused line

  Net quantity statement missing

  The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

• 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.

• USUAL NAME1 refused line

  Common or usual name missing

  The label appeared not to show the common or usual name of the food.

Questions about Cartier Saada SA

Is Cartier Saada SA on an FDA import alert?

No listing for Cartier Saada SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Morocco page.

Has FDA refused shipments from Cartier Saada SA?

Yes. FDA refused 8 shipment lines from Cartier Saada SA between December 19, 2017 and August 24, 2020. The most recent, on August 24, 2020, was artichoke (leaf & stem vegetable), charged as NO PROCESS (no scheduled process filed).

Why did FDA refuse Cartier Saada SA's shipments?

The most frequent charges are NUTRIT LBL (nutrition information missing from label, 6 lines) and NO PROCESS (no scheduled process filed, 5 lines).

When was Cartier Saada SA last inspected by FDA?

FDA's most recent inspection of Cartier Saada SA with a final classification is dated May 12, 2018 and was classified VAI (Voluntary Action Indicated).

What is Cartier Saada SA's FEI number?

Cartier Saada SA's FDA Establishment Identifier (FEI) is 3009212103.