Umeken Co. Ltd. (Toyoma Factory #1)
FDA import alert and refusal historyToyama, JapanFEI 3004336163
As of October 26, 2026, Umeken Co. Ltd. (Toyoma Factory #1) has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on October 24, 2019, 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 Umeken Co. Ltd. (Toyoma Factory #1)
4 records, newest first. Each line links to the FDA page it came from.
2019
2012
Questions about Umeken Co. Ltd. (Toyoma Factory #1)
- Is Umeken Co. Ltd. (Toyoma Factory #1) on an FDA import alert?
- No listing for Umeken Co. Ltd. (Toyoma Factory #1) 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 Umeken Co. Ltd. (Toyoma Factory #1)?
- No FDA import refusals for Umeken Co. Ltd. (Toyoma Factory #1) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Umeken Co. Ltd. (Toyoma Factory #1) last inspected by FDA?
- FDA's most recent inspection of Umeken Co. Ltd. (Toyoma Factory #1) with a final classification is dated October 24, 2019 and was classified NAI (No Action Indicated).
- What is Umeken Co. Ltd. (Toyoma Factory #1)'s FEI number?
- Umeken Co. Ltd. (Toyoma Factory #1)'s FDA Establishment Identifier (FEI) is 3004336163.
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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.