Pt. Varia Niaga Nusantara
FDA import alert and refusal historyPasuruan, IndonesiaFEI 3004249162
As of October 26, 2026, Pt. Varia Niaga Nusantara (Pasuruan, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tuna, published by FDA on February 14, 2011, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Pt. Varia Niaga Nusantara
3 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 16-81red listTunaSource
Questions about Pt. Varia Niaga Nusantara
- Is Pt. Varia Niaga Nusantara on an FDA import alert?
- Yes. As of October 26, 2026, Pt. Varia Niaga Nusantara is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tuna; FDA published the listing on February 14, 2011.
- Has FDA refused shipments from Pt. Varia Niaga Nusantara?
- No FDA import refusals for Pt. Varia Niaga Nusantara appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Pt. Varia Niaga Nusantara last inspected by FDA?
- FDA's most recent inspection of Pt. Varia Niaga Nusantara with a final classification is dated January 9, 2018 and was classified NAI (No Action Indicated).
- What is Pt. Varia Niaga Nusantara's FEI number?
- Pt. Varia Niaga Nusantara's FDA Establishment Identifier (FEI) is 3004249162.
- Can shipments from Pt. Varia Niaga Nusantara still enter the U.S.?
- Shipments of tuna from Pt. Varia Niaga Nusantara can be detained without physical examination under Import Alert 16-81; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.