Kien Hung

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

Refusal charges, in plain English

• SALMONELLA4 refused lines

  Salmonella

  The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

• VETDRUGRES2 refused lines

  Animal drug residue

  The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.

Questions about Kien Hung

Is Kien Hung on an FDA import alert?

Yes. As of October 25, 2026, Kien Hung is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for featherback fish paste; FDA published the listing on November 26, 2019.

Has FDA refused shipments from Kien Hung?

Yes. FDA refused 6 shipment lines from Kien Hung between February 16, 2017 and May 13, 2020. The most recent, on May 13, 2020, was fish paste, fishery products, n.e.c., charged as SALMONELLA (salmonella).

Why did FDA refuse Kien Hung's shipments?

The most frequent charges are SALMONELLA (salmonella, 4 lines) and VETDRUGRES (animal drug residue, 2 lines).

When was Kien Hung last inspected by FDA?

FDA's most recent inspection of Kien Hung with a final classification is dated February 22, 2019 and was classified VAI (Voluntary Action Indicated).

What is Kien Hung's FEI number?

Kien Hung's FDA Establishment Identifier (FEI) is 3004352756.

Can shipments from Kien Hung still enter the U.S.?

Shipments of featherback fish paste from Kien Hung can be detained without physical examination under Import Alert 16-81; 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).