Alberto De Miguel S.A.

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

Refusal charges, in plain English

• 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.

• 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 Alberto De Miguel S.A.

Is Alberto De Miguel S.A. on an FDA import alert?

Yes. As of October 25, 2026, Alberto De Miguel S.A. is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for asparagus (whole) in brine; asparagus in brine (whole); FDA published the listing on June 3, 2014.

Has FDA refused shipments from Alberto De Miguel S.A.?

Yes. FDA refused 1 shipment line from Alberto De Miguel S.A. on March 17, 2022. The most recent, on March 17, 2022, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as NO ENGLISH (required label information not in english).

Why did FDA refuse Alberto De Miguel S.A.'s shipments?

The most frequent charges are NO ENGLISH (required label information not in english, 1 line) and NO PROCESS (no scheduled process filed, 1 line).

When was Alberto De Miguel S.A. last inspected by FDA?

FDA's most recent inspection of Alberto De Miguel S.A. with a final classification is dated May 10, 2023 and was classified VAI (Voluntary Action Indicated).

What is Alberto De Miguel S.A.'s FEI number?

Alberto De Miguel S.A.'s FDA Establishment Identifier (FEI) is 8976.

Can shipments from Alberto De Miguel S.A. still enter the U.S.?

Shipments of asparagus (whole) in brine; asparagus in brine (whole) from Alberto De Miguel S.A. can be detained without physical examination under Import Alert 99-37; 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).