Meysu Gida San. ve Tic.

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

Refusal charges, in plain English

• POISONOUS2 refused lines

  Poisonous or deleterious substance

  The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

• 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 Meysu Gida San. ve Tic.

Is Meysu Gida San. ve Tic. on an FDA import alert?

Yes. As of October 26, 2026, Meysu Gida San. ve Tic. is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for apple juice; 100% natural; FDA published the listing on October 14, 2022.

Has FDA refused shipments from Meysu Gida San. ve Tic.?

Yes. FDA refused 3 shipment lines from Meysu Gida San. ve Tic. between May 30, 2019 and February 20, 2025. The most recent, on February 20, 2025, was beverage base, combination true fruit and imitation fruit flavors, liquid (not cocktail or punch), charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse Meysu Gida San. ve Tic.'s shipments?

The most frequent charges are POISONOUS (poisonous or deleterious substance, 2 lines) and NEEDS FCE (processor not registered for canned or acidified foods, 1 line).

What is Meysu Gida San. ve Tic.'s FEI number?

Meysu Gida San. ve Tic.'s FDA Establishment Identifier (FEI) is 3011365911.

Can shipments from Meysu Gida San. ve Tic. still enter the U.S.?

Shipments of apple juice; 100% natural from Meysu Gida San. ve Tic. can be detained without physical examination under Import Alert 99-42; 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).