Manuel Romero de Avila Ramirez S.A.

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 LBLG1 refused line

  Artificial coloring not declared

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

• SUBSTITUTE1 refused line

  SUBSTITUTE

Questions about Manuel Romero de Avila Ramirez S.A.

Is Manuel Romero de Avila Ramirez S.A. on an FDA import alert?

No listing for Manuel Romero de Avila Ramirez S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.

Has FDA refused shipments from Manuel Romero de Avila Ramirez S.A.?

Yes. FDA refused 5 shipment lines from Manuel Romero de Avila Ramirez S.A. between August 7, 2020 and April 29, 2021. The most recent, on April 29, 2021, was saffron, whole (spice), charged as COLOR LBLG (artificial coloring not declared).

Why did FDA refuse Manuel Romero de Avila Ramirez S.A.'s shipments?

The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 4 lines) and COLOR LBLG (artificial coloring not declared, 1 line).

When was Manuel Romero de Avila Ramirez S.A. last inspected by FDA?

FDA's most recent inspection of Manuel Romero de Avila Ramirez S.A. with a final classification is dated June 21, 2018 and was classified NAI (No Action Indicated).

What is Manuel Romero de Avila Ramirez S.A.'s FEI number?

Manuel Romero de Avila Ramirez S.A.'s FDA Establishment Identifier (FEI) is 3010122881.