Sansyokuhin Co., Ltd.

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

Refusal charges, in plain English

• NO PROCESS12 refused lines

  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.

• NEEDS FCE5 refused lines

  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.

Questions about Sansyokuhin Co., Ltd.

Is Sansyokuhin Co., Ltd. on an FDA import alert?

Yes. As of October 26, 2026, Sansyokuhin Co., Ltd. is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for all shelf stable konjac noodle products (pastas); FDA published the listing on October 16, 2023.

Has FDA refused shipments from Sansyokuhin Co., Ltd.?

Yes. FDA refused 12 shipment lines from Sansyokuhin Co., Ltd. on September 18, 2023. The most recent, on September 18, 2023, was oriental noodles (flavored with shrimp,chicken,beef,lobster,crab,plain,etc.), charged as NO PROCESS (no scheduled process filed).

Why did FDA refuse Sansyokuhin Co., Ltd.'s shipments?

The most frequent charges are NO PROCESS (no scheduled process filed, 12 lines) and NEEDS FCE (processor not registered for canned or acidified foods, 5 lines).

What is Sansyokuhin Co., Ltd.'s FEI number?

Sansyokuhin Co., Ltd.'s FDA Establishment Identifier (FEI) is 3001177259.

Can shipments from Sansyokuhin Co., Ltd. still enter the U.S.?

Shipments of all shelf stable konjac noodle products (pastas) from Sansyokuhin Co., Ltd. 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).