Has FDA refused shipments from EIWA Marine Products, Inc.?

No FDA import refusals for EIWA Marine Products, Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.

When was EIWA Marine Products, Inc. last inspected by FDA?

FDA's most recent inspection of EIWA Marine Products, Inc. with a final classification is dated January 18, 2020 and was classified VAI (Voluntary Action Indicated).

What is EIWA Marine Products, Inc.'s FEI number?

EIWA Marine Products, Inc.'s FDA Establishment Identifier (FEI) is 3010733139.

Can shipments from EIWA Marine Products, Inc. still enter the U.S.?

Shipments of barracuda; eel; sardines; amberjack (kampachi) from EIWA Marine Products, Inc. can be detained without physical examination under Import Alert 16-119; 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).

EIWA Marine Products, Inc.

FDA import alert and refusal historyChuo, JapanFEI 3010733139

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As of October 26, 2026, EIWA Marine Products, Inc. (Chuo, Japan) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for barracuda; eel; sardines; amberjack (kampachi), published by FDA on April 26, 2011, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: IA 16-119 · red list
Last import refusal: None since October 2016
Last warning letter: None found
Last inspection: Jan 18, 2020Classified VAI (Voluntary Action Indicated)

Every FDA record for EIWA Marine Products, Inc.

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

2020

Jan 18, 2020Inspection
Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
Source

2011

Apr 26, 2011Import alert listing
Listed on Import Alert 16-119red listBarracuda; Eel; Sardines; Amberjack (Kampachi)
Source

Questions about EIWA Marine Products, Inc.

Is EIWA Marine Products, Inc. on an FDA import alert?: Yes. As of October 26, 2026, EIWA Marine Products, Inc. is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for barracuda; eel; sardines; amberjack (kampachi); FDA published the listing on April 26, 2011.
Has FDA refused shipments from EIWA Marine Products, Inc.?: No FDA import refusals for EIWA Marine Products, Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was EIWA Marine Products, Inc. last inspected by FDA?: FDA's most recent inspection of EIWA Marine Products, Inc. with a final classification is dated January 18, 2020 and was classified VAI (Voluntary Action Indicated).
What is EIWA Marine Products, Inc.'s FEI number?: EIWA Marine Products, Inc.'s FDA Establishment Identifier (FEI) is 3010733139.
Can shipments from EIWA Marine Products, Inc. still enter the U.S.?: Shipments of barracuda; eel; sardines; amberjack (kampachi) from EIWA Marine Products, Inc. can be detained without physical examination under Import Alert 16-119; 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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