PT.Keong Nusantara Abadi
FDA import alert and refusal historyKediri, IndonesiaFEI 3004254997
As of October 26, 2026, PT.Keong Nusantara Abadi has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 19, 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 PT.Keong Nusantara Abadi
2 records, newest first. Each line links to the FDA page it came from.
Questions about PT.Keong Nusantara Abadi
- Is PT.Keong Nusantara Abadi on an FDA import alert?
- No listing for PT.Keong Nusantara Abadi appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
- Has FDA refused shipments from PT.Keong Nusantara Abadi?
- No FDA import refusals for PT.Keong Nusantara Abadi appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was PT.Keong Nusantara Abadi last inspected by FDA?
- FDA's most recent inspection of PT.Keong Nusantara Abadi with a final classification is dated January 19, 2018 and was classified VAI (Voluntary Action Indicated).
- What is PT.Keong Nusantara Abadi's FEI number?
- PT.Keong Nusantara Abadi's FDA Establishment Identifier (FEI) is 3004254997.
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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.