Triko Foods Co., Ltd Factory 3

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.

• STD IDENT1 refused line

  Does not conform to standard of identity

  The product appeared to be represented as a food that has an FDA standard of identity, but not to conform to that standard.

• STD NAME1 refused line

  STD NAME

Questions about Triko Foods Co., Ltd Factory 3

Is Triko Foods Co., Ltd Factory 3 on an FDA import alert?

Yes. As of October 27, 2026, Triko Foods Co., Ltd Factory 3 is on the red list of FDA Import Alert 33-15, “Mini-cup gel and jelly candies of firm consistency”, for dr. q grape konjac fruit jelly; dr. q peach / white grape konjac fruit jelly; FDA published the listing on August 4, 2026.

Has FDA refused shipments from Triko Foods Co., Ltd Factory 3?

Yes. FDA refused 1 shipment line from Triko Foods Co., Ltd Factory 3 on June 30, 2025. The most recent, on June 30, 2025, was peanut, shelled, charged as STD IDENT (does not conform to standard of identity).

Why did FDA refuse Triko Foods Co., Ltd Factory 3's shipments?

The most frequent charges are NO ENGLISH (required label information not in english, 1 line) and STD IDENT (does not conform to standard of identity, 1 line).

When was Triko Foods Co., Ltd Factory 3 last inspected by FDA?

FDA's most recent inspection of Triko Foods Co., Ltd Factory 3 with a final classification is dated March 14, 2018 and was classified NAI (No Action Indicated).

What is Triko Foods Co., Ltd Factory 3's FEI number?

Triko Foods Co., Ltd Factory 3's FDA Establishment Identifier (FEI) is 3013274311.

Can shipments from Triko Foods Co., Ltd Factory 3 still enter the U.S.?

Shipments of dr. q grape konjac fruit jelly; dr. q peach / white grape konjac fruit jelly from Triko Foods Co., Ltd Factory 3 can be detained without physical examination under Import Alert 33-15; 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).