Alipro AG

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

Refusal charges, in plain English

• UNSAFE COL4 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 LBLG3 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.

Questions about Alipro AG

Is Alipro AG on an FDA import alert?

No listing for Alipro AG appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Switzerland page.

Has FDA refused shipments from Alipro AG?

Yes. FDA refused 4 shipment lines from Alipro AG on September 6, 2019. The most recent, on September 6, 2019, was icings and icing mixes, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Alipro AG's shipments?

The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 4 lines) and COLOR LBLG (artificial coloring not declared, 3 lines).

When was Alipro AG last inspected by FDA?

FDA's most recent inspection of Alipro AG with a final classification is dated April 17, 2026 and was classified VAI (Voluntary Action Indicated).

What is Alipro AG's FEI number?

Alipro AG's FDA Establishment Identifier (FEI) is 3004321179.