Kans Pacific Sea Product Co
FDA import alert and refusal historyHong Kong, Hong KongFEI 1000340304
As of October 26, 2026, Kans Pacific Sea Product Co (Hong Kong, Hong Kong) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for dried abalone; abalone, breaded, plastic, synth, ntrl/artfcl dried, published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kans Pacific Sea Product Co
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listDried abalone; Abalone, Breaded, Plastic, Synth, Ntrl/Artfcl DriedSource
Questions about Kans Pacific Sea Product Co
- Is Kans Pacific Sea Product Co on an FDA import alert?
- Yes. As of October 26, 2026, Kans Pacific Sea Product Co is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for dried abalone; abalone, breaded, plastic, synth, ntrl/artfcl dried; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Kans Pacific Sea Product Co?
- No FDA import refusals for Kans Pacific Sea Product Co appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kans Pacific Sea Product Co's FEI number?
- Kans Pacific Sea Product Co's FDA Establishment Identifier (FEI) is 1000340304.
- Can shipments from Kans Pacific Sea Product Co still enter the U.S.?
- Shipments of dried abalone; abalone, breaded, plastic, synth, ntrl/artfcl dried from Kans Pacific Sea Product Co 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).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.