PT. Muria Bahari Indonesia
FDA import alert and refusal historyKudus, IndonesiaFEI 3011280608
As of October 26, 2026, PT. Muria Bahari Indonesia has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on July 18, 2017, 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. Muria Bahari Indonesia
2 records, newest first. Each line links to the FDA page it came from.
Questions about PT. Muria Bahari Indonesia
- Is PT. Muria Bahari Indonesia on an FDA import alert?
- No listing for PT. Muria Bahari Indonesia 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. Muria Bahari Indonesia?
- No FDA import refusals for PT. Muria Bahari Indonesia appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was PT. Muria Bahari Indonesia last inspected by FDA?
- FDA's most recent inspection of PT. Muria Bahari Indonesia with a final classification is dated July 18, 2017 and was classified VAI (Voluntary Action Indicated).
- What is PT. Muria Bahari Indonesia's FEI number?
- PT. Muria Bahari Indonesia's FDA Establishment Identifier (FEI) is 3011280608.
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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.