Maruhachi Muramatsu Inc., Danchi Factory
FDA import alert and refusal historyYaizu, JapanFEI 3004680255
As of October 26, 2026, Maruhachi Muramatsu Inc., Danchi Factory has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on April 24, 2024, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)
Every FDA record for Maruhachi Muramatsu Inc., Danchi Factory
2 records, newest first. Each line links to the FDA page it came from.
Questions about Maruhachi Muramatsu Inc., Danchi Factory
- Is Maruhachi Muramatsu Inc., Danchi Factory on an FDA import alert?
- No listing for Maruhachi Muramatsu Inc., Danchi Factory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Maruhachi Muramatsu Inc., Danchi Factory?
- No FDA import refusals for Maruhachi Muramatsu Inc., Danchi Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
- Has Maruhachi Muramatsu Inc., Danchi Factory received an FDA warning letter?
- Yes. FDA issued a warning letter to Maruhachi Muramatsu Inc., Danchi Factory on October 17, 2024 (Seafood HACCP/CGMP for Foods/Adulterated).
- When was Maruhachi Muramatsu Inc., Danchi Factory last inspected by FDA?
- FDA's most recent inspection of Maruhachi Muramatsu Inc., Danchi Factory with a final classification is dated April 24, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Maruhachi Muramatsu Inc., Danchi Factory's FEI number?
- Maruhachi Muramatsu Inc., Danchi Factory's FDA Establishment Identifier (FEI) is 3004680255.
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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.