Grupo Jumex Mexicali Planta II

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

Refusal charges, in plain English

• NEEDS FCE1 refused line

  Processor not registered for canned or acidified foods

  The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

• NO PROCESS1 refused line

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Grupo Jumex Mexicali Planta II

Is Grupo Jumex Mexicali Planta II on an FDA import alert?

Yes. As of October 26, 2026, Grupo Jumex Mexicali Planta II is on the green list of FDA Import Alert 21-07, “Tamarind and tamarind products: filth”, for tamarind beverage kerns tamarind flavored; beverage; FDA published the listing on October 3, 2011.

Has FDA refused shipments from Grupo Jumex Mexicali Planta II?

Yes. FDA refused 1 shipment line from Grupo Jumex Mexicali Planta II on September 15, 2017. The most recent, on September 15, 2017, was papaya (papaw), juice, milk, creme, drink or nectar, sub/tropical fruit, charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse Grupo Jumex Mexicali Planta II's shipments?

The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 1 line) and NO PROCESS (no scheduled process filed, 1 line).

When was Grupo Jumex Mexicali Planta II last inspected by FDA?

FDA's most recent inspection of Grupo Jumex Mexicali Planta II with a final classification is dated April 4, 2019 and was classified NAI (No Action Indicated).

What is Grupo Jumex Mexicali Planta II's FEI number?

Grupo Jumex Mexicali Planta II's FDA Establishment Identifier (FEI) is 3005210422.