Proamex Internacional S.A.P.I. De C.V.

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

Refusal charges, in plain English

• COLOR LBLG6 refused lines

  Artificial coloring not declared

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

• 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.

Questions about Proamex Internacional S.A.P.I. De C.V.

Is Proamex Internacional S.A.P.I. De C.V. on an FDA import alert?

Yes. As of October 26, 2026, Proamex Internacional S.A.P.I. De C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for blackberry tamale (tamal zarzamora); frozen guava tamales; strawberry tamale (tamal fresa); FDA published the listing on December 4, 2018.

Has FDA refused shipments from Proamex Internacional S.A.P.I. De C.V.?

Yes. FDA refused 6 shipment lines from Proamex Internacional S.A.P.I. De C.V. between December 12, 2018 and August 20, 2019. The most recent, on August 20, 2019, was pastry (other than fruit or jelly filled) without custard or cream filling, charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Proamex Internacional S.A.P.I. De C.V.'s shipments?

The most frequent charges are COLOR LBLG (artificial coloring not declared, 6 lines) and UNSAFE COL (color additive unsafe under section 721, 6 lines).

What is Proamex Internacional S.A.P.I. De C.V.'s FEI number?

Proamex Internacional S.A.P.I. De C.V.'s FDA Establishment Identifier (FEI) is 3012242924.

Can shipments from Proamex Internacional S.A.P.I. De C.V. still enter the U.S.?

Shipments of blackberry tamale (tamal zarzamora); frozen guava tamales; strawberry tamale (tamal fresa) from Proamex Internacional S.A.P.I. 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).