Sanuki Kanzume Co., Akita Plant
FDA import alert and refusal historyYurihonjo, JapanFEI 3004686576
Recorded by FDA as SANUKI KANZUME CO., AKITA PLANT
As of October 27, 2026, Sanuki Kanzume Co., Akita Plant has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 19, 2017, 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 Sanuki Kanzume Co., Akita Plant
2 records, newest first. Each line links to the FDA page it came from.
Questions about Sanuki Kanzume Co., Akita Plant
- Is Sanuki Kanzume Co., Akita Plant on an FDA import alert?
- No listing for Sanuki Kanzume Co., Akita Plant appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Sanuki Kanzume Co., Akita Plant?
- No FDA import refusals for Sanuki Kanzume Co., Akita Plant appear in FDA's refusal data since October 2016, as of October 27, 2026.
- When was Sanuki Kanzume Co., Akita Plant last inspected by FDA?
- FDA's most recent inspection of Sanuki Kanzume Co., Akita Plant with a final classification is dated May 19, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Sanuki Kanzume Co., Akita Plant's FEI number?
- Sanuki Kanzume Co., Akita Plant's FDA Establishment Identifier (FEI) is 3004686576.
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