Hidecho Suisan Co., Ltd.
FDA import alert and refusal historyUwajima, JapanFEI 3006577589
Recorded by FDA as HIDECHO SUISAN CO., LTD.
As of October 25, 2026, Hidecho Suisan Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 29, 2019, 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
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Hidecho Suisan Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Hidecho Suisan Co., Ltd.
- Is Hidecho Suisan Co., Ltd. on an FDA import alert?
- No listing for Hidecho Suisan 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 Hidecho Suisan Co., Ltd.?
- No FDA import refusals for Hidecho Suisan Co., Ltd. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Hidecho Suisan Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Hidecho Suisan Co., Ltd. with a final classification is dated January 29, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Hidecho Suisan Co., Ltd.'s FEI number?
- Hidecho Suisan Co., Ltd.'s FDA Establishment Identifier (FEI) is 3006577589.
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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.