Kuki Sangyo Co., Ltd.
FDA import alert and refusal historyYokkaichi, JapanFEI 1000272783
As of October 26, 2026, Kuki Sangyo Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on February 26, 2018, 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 Kuki Sangyo Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Kuki Sangyo Co., Ltd.
- Is Kuki Sangyo Co., Ltd. on an FDA import alert?
- No listing for Kuki Sangyo 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 Kuki Sangyo Co., Ltd.?
- No FDA import refusals for Kuki Sangyo Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Kuki Sangyo Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Kuki Sangyo Co., Ltd. with a final classification is dated February 26, 2018 and was classified NAI (No Action Indicated).
- What is Kuki Sangyo Co., Ltd.'s FEI number?
- Kuki Sangyo Co., Ltd.'s FDA Establishment Identifier (FEI) is 1000272783.
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