P.t. Surya Terbit Co.,ltd.
FDA import alert and refusal historyPhuket, ThailandFEI 3006731451
As of October 26, 2026, P.t. Surya Terbit Co.,ltd. (Phuket, Thailand) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for tuna, published by FDA on April 23, 2010, 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 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for P.t. Surya Terbit Co.,ltd.
2 records, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 16-120red listTunaSource
2009
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about P.t. Surya Terbit Co.,ltd.
- Is P.t. Surya Terbit Co.,ltd. on an FDA import alert?
- Yes. As of October 26, 2026, P.t. Surya Terbit Co.,ltd. is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for tuna; FDA published the listing on April 23, 2010.
- Has FDA refused shipments from P.t. Surya Terbit Co.,ltd.?
- No FDA import refusals for P.t. Surya Terbit Co.,ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was P.t. Surya Terbit Co.,ltd. last inspected by FDA?
- FDA's most recent inspection of P.t. Surya Terbit Co.,ltd. with a final classification is dated December 4, 2009 and was classified OAI (Official Action Indicated).
- What is P.t. Surya Terbit Co.,ltd.'s FEI number?
- P.t. Surya Terbit Co.,ltd.'s FDA Establishment Identifier (FEI) is 3006731451.
- Can shipments from P.t. Surya Terbit Co.,ltd. still enter the U.S.?
- Shipments of tuna from P.t. Surya Terbit Co.,ltd. can be detained without physical examination under Import Alert 16-120; 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.