Productos Techani SA de CV

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

Refusal charges, in plain English

• LIST INGRE2 refused lines

  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).

• 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.

• NO ENGLISH1 refused line

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• 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.

• 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 Productos Techani SA de CV

Is Productos Techani SA de CV on an FDA import alert?

No listing for Productos Techani SA de CV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.

Has FDA refused shipments from Productos Techani SA de CV?

Yes. FDA refused 2 shipment lines from Productos Techani SA de CV between October 14, 2016 and January 2, 2019. The most recent, on January 2, 2019, was candy specialties, n.e.c. (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Productos Techani SA de CV's shipments?

The most frequent charges are LIST INGRE (ingredients not listed, 2 lines) and LACKS FIRM (manufacturer name and address missing, 1 line).

When was Productos Techani SA de CV last inspected by FDA?

FDA's most recent inspection of Productos Techani SA de CV with a final classification is dated January 26, 2026 and was classified VAI (Voluntary Action Indicated).

What is Productos Techani SA de CV's FEI number?

Productos Techani SA de CV's FDA Establishment Identifier (FEI) is 3010631261.