AMAKUSA GYOEN Co., Ltd
FDA import alert and refusal historyAmakusa, JapanFEI 3004257484
As of October 26, 2026, AMAKUSA GYOEN Co., Ltd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on February 27, 2025, was classified NAI (No 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 NAI (No Action Indicated)
Every FDA record for AMAKUSA GYOEN Co., Ltd
2 records, newest first. Each line links to the FDA page it came from.
Questions about AMAKUSA GYOEN Co., Ltd
- Is AMAKUSA GYOEN Co., Ltd on an FDA import alert?
- No listing for AMAKUSA GYOEN Co., Ltd 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 AMAKUSA GYOEN Co., Ltd?
- No FDA import refusals for AMAKUSA GYOEN Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was AMAKUSA GYOEN Co., Ltd last inspected by FDA?
- FDA's most recent inspection of AMAKUSA GYOEN Co., Ltd with a final classification is dated February 27, 2025 and was classified NAI (No Action Indicated).
- What is AMAKUSA GYOEN Co., Ltd's FEI number?
- AMAKUSA GYOEN Co., Ltd's FDA Establishment Identifier (FEI) is 3004257484.
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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.