Deiman, S.A. de C.V.

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

Refusal charges, in plain English

• LABELING24 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.

• UNSAFE COL6 refused lines

  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.

• COLOR LBLG5 refused lines

  Artificial coloring not declared

  The product appeared to contain an artificial coloring without labeling that states that fact.

• COLORLABEL1 refused line

  Required information not prominent

  Information required on the label appeared not to be placed prominently enough, or in such terms, to be read and understood by an ordinary consumer.

• 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 Deiman, S.A. de C.V.

Is Deiman, S.A. de C.V. on an FDA import alert?

Yes. As of October 26, 2026, Deiman, S.A. de C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for artificial food color orange yellow 370 l (for food use); FDA published the listing on June 22, 2017.

Has FDA refused shipments from Deiman, S.A. de C.V.?

Yes. FDA refused 31 shipment lines from Deiman, S.A. de C.V. between May 4, 2017 and August 19, 2026. The most recent, on August 19, 2026, was color adjuncts (food additives for human use), charged as COLOR LBLG (artificial coloring not declared).

Why did FDA refuse Deiman, S.A. de C.V.'s shipments?

The most frequent charges are LABELING (fair packaging and labeling act, 24 lines) and UNSAFE COL (color additive unsafe under section 721, 6 lines).

When was Deiman, S.A. de C.V. last inspected by FDA?

FDA's most recent inspection of Deiman, S.A. de C.V. with a final classification is dated August 24, 2018 and was classified VAI (Voluntary Action Indicated).

What is Deiman, S.A. de C.V.'s FEI number?

Deiman, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004483157.

Can shipments from Deiman, S.A. de C.V. still enter the U.S.?

Shipments of artificial food color orange yellow 370 l (for food use) from Deiman, S.A. de C.V. 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).