Yamamori Inc. Matsuzaka Factory
FDA import alert and refusal historyMatsusaka, JapanFEI 3009905495
Recorded by FDA as YAMAMORI INC. MATSUZAKA FACTORY
As of October 26, 2026, Yamamori Inc. Matsuzaka Factory has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on February 5, 2015, 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 Yamamori Inc. Matsuzaka Factory
2 records, newest first. Each line links to the FDA page it came from.
Questions about Yamamori Inc. Matsuzaka Factory
- Is Yamamori Inc. Matsuzaka Factory on an FDA import alert?
- No listing for Yamamori Inc. Matsuzaka 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 Yamamori Inc. Matsuzaka Factory?
- No FDA import refusals for Yamamori Inc. Matsuzaka Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Yamamori Inc. Matsuzaka Factory last inspected by FDA?
- FDA's most recent inspection of Yamamori Inc. Matsuzaka Factory with a final classification is dated February 5, 2015 and was classified VAI (Voluntary Action Indicated).
- What is Yamamori Inc. Matsuzaka Factory's FEI number?
- Yamamori Inc. Matsuzaka Factory's FDA Establishment Identifier (FEI) is 3009905495.
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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.