Sanko Seika Co., Ltd. Niizaki Factory
FDA import alert and refusal historyNiigata, JapanFEI 1000193554
As of October 26, 2026, Sanko Seika Co., Ltd. Niizaki Factory has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on February 20, 2018, 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 Sanko Seika Co., Ltd. Niizaki Factory
2 records, newest first. Each line links to the FDA page it came from.
Questions about Sanko Seika Co., Ltd. Niizaki Factory
- Is Sanko Seika Co., Ltd. Niizaki Factory on an FDA import alert?
- No listing for Sanko Seika Co., Ltd. Niizaki 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 Sanko Seika Co., Ltd. Niizaki Factory?
- No FDA import refusals for Sanko Seika Co., Ltd. Niizaki Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sanko Seika Co., Ltd. Niizaki Factory last inspected by FDA?
- FDA's most recent inspection of Sanko Seika Co., Ltd. Niizaki Factory with a final classification is dated February 20, 2018 and was classified VAI (Voluntary Action Indicated).
- What is Sanko Seika Co., Ltd. Niizaki Factory's FEI number?
- Sanko Seika Co., Ltd. Niizaki Factory's FDA Establishment Identifier (FEI) is 1000193554.
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