Bach Thao Co., Ltd.
FDA import alert and refusal historyLong Xuyen City, VietnamFEI 3005139068
As of October 25, 2026, Bach Thao Co., Ltd. (Long Xuyen City, Vietnam) is on the red list of FDA Import Alert 16-04 (Seafood products that appear to be misbranded) for tilapia; tilapia, aquaculture harvested fishery/seafood products, published by FDA on September 18, 2009, 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 16-04 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Bach Thao Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-04red listTilapia; Tilapia, Aquaculture Harvested Fishery/Seafood ProductsSource
Questions about Bach Thao Co., Ltd.
- Is Bach Thao Co., Ltd. on an FDA import alert?
- Yes. As of October 25, 2026, Bach Thao Co., Ltd. is on the red list of FDA Import Alert 16-04, “Seafood products that appear to be misbranded”, for tilapia; tilapia, aquaculture harvested fishery/seafood products; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Bach Thao Co., Ltd.?
- No FDA import refusals for Bach Thao Co., Ltd. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Bach Thao Co., Ltd.'s FEI number?
- Bach Thao Co., Ltd.'s FDA Establishment Identifier (FEI) is 3005139068.
- Can shipments from Bach Thao Co., Ltd. still enter the U.S.?
- Shipments of tilapia; tilapia, aquaculture harvested fishery/seafood products from Bach Thao Co., Ltd. can be detained without physical examination under Import Alert 16-04; 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.