Tomita Pharmaceutical Co., Ltd.
FDA import alert and refusal historyNaruto, JapanFEI 3002808375
As of October 26, 2026, Tomita Pharmaceutical Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on November 1, 2013, 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 Tomita Pharmaceutical Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Tomita Pharmaceutical Co., Ltd.
- Is Tomita Pharmaceutical Co., Ltd. on an FDA import alert?
- No listing for Tomita Pharmaceutical 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 Tomita Pharmaceutical Co., Ltd.?
- No FDA import refusals for Tomita Pharmaceutical Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Tomita Pharmaceutical Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Tomita Pharmaceutical Co., Ltd. with a final classification is dated November 1, 2013 and was classified VAI (Voluntary Action Indicated).
- What is Tomita Pharmaceutical Co., Ltd.'s FEI number?
- Tomita Pharmaceutical Co., Ltd.'s FDA Establishment Identifier (FEI) is 3002808375.
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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.