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Marumo Co., Ltd.

FDA import alert and refusal historyKagoshima, JapanFEI 3008410019

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Example subjectMarumo Co., Ltd added to Import Alert 16-129 (red list)

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As of October 25, 2026, Marumo Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 26, 2023, was classified OAI (Official Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
Seafood HACCP/CGMP for Foods/Adulterated
Last inspection
Classified OAI (Official Action Indicated)

Every FDA record for Marumo Co., Ltd.

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

2023

  1. Warning letter
    Warning letter issuedSeafood HACCP/CGMP for Foods/Adulterated
    Source
  2. Inspection
    Inspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Marumo Co., Ltd.

Is Marumo Co., Ltd. on an FDA import alert?
No listing for Marumo Co., Ltd. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Japan page.
Has FDA refused shipments from Marumo Co., Ltd.?
No FDA import refusals for Marumo Co., Ltd. appear in FDA's refusal data since October 2016, as of October 25, 2026.
Has Marumo Co., Ltd. received an FDA warning letter?
Yes. FDA issued a warning letter to Marumo Co., Ltd. on June 30, 2023 (Seafood HACCP/CGMP for Foods/Adulterated).
When was Marumo Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Marumo Co., Ltd. with a final classification is dated January 26, 2023 and was classified OAI (Official Action Indicated).
What is Marumo Co., Ltd.'s FEI number?
Marumo Co., Ltd.'s FDA Establishment Identifier (FEI) is 3008410019.

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Example subjectMarumo Co., Ltd 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.