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Maruha Nichiro Corporation

FDA import alert and refusal historyUtsunomiya, JapanFEI 1000421992

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Example subjectMaruha Nichiro Corporatio added to Import Alert 16-129 (red list)

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As of October 26, 2026, Maruha Nichiro Corporation is on the green list of FDA Import Alert 16-02, which exempts its listed products from detention without physical examination under that alert, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Maruha Nichiro Corporation

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

2016

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Monitoring of Marketed Animal Drugs, Feed, and Devices
    Source

2009

  1. Import alert listing
    Listed on Import Alert 16-02green listShark Cartilage Concentrate
    Source

Questions about Maruha Nichiro Corporation

Is Maruha Nichiro Corporation on an FDA import alert?
Yes. As of October 26, 2026, Maruha Nichiro Corporation is on the green list of FDA Import Alert 16-02, “Dried shark fins, fish maws and shark cartilage: filth”, for shark cartilage concentrate; FDA published the listing on September 10, 2009.
Has FDA refused shipments from Maruha Nichiro Corporation?
No FDA import refusals for Maruha Nichiro Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Maruha Nichiro Corporation last inspected by FDA?
FDA's most recent inspection of Maruha Nichiro Corporation with a final classification is dated February 26, 2016 and was classified VAI (Voluntary Action Indicated).
What is Maruha Nichiro Corporation's FEI number?
Maruha Nichiro Corporation's FDA Establishment Identifier (FEI) is 1000421992.

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Example subjectMaruha Nichiro Corporatio added to Import Alert 16-129 (red list)

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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.