Sai Thanh Co. Ltd
FDA import alert and refusal historyHo Chi Minh City, VietnamFEI 3011786799
As of October 26, 2026, Sai Thanh Co. Ltd (Ho Chi Minh City, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for bonito (wild caught), published by FDA on December 4, 2019, 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 VAI (Voluntary Action Indicated)
Every FDA record for Sai Thanh Co. Ltd
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import alert listingListed on Import Alert 16-81red listBonito (Wild Caught)Source
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Sai Thanh Co. Ltd
- Is Sai Thanh Co. Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Sai Thanh Co. Ltd is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for bonito (wild caught); FDA published the listing on December 4, 2019.
- Has FDA refused shipments from Sai Thanh Co. Ltd?
- No FDA import refusals for Sai Thanh Co. Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sai Thanh Co. Ltd last inspected by FDA?
- FDA's most recent inspection of Sai Thanh Co. Ltd with a final classification is dated March 6, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Sai Thanh Co. Ltd's FEI number?
- Sai Thanh Co. Ltd's FDA Establishment Identifier (FEI) is 3011786799.
- Can shipments from Sai Thanh Co. Ltd still enter the U.S.?
- Shipments of bonito (wild caught) from Sai Thanh Co. Ltd 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.