Cafatex Fishery Joint Stock Corporation
FDA import alert and refusal historyTay Ninh, VietnamFEI 3004300892
Recorded by FDA as CAFATEX FISHERY JOINT STOCK CORPORATION
As of October 26, 2026, Cafatex Fishery Joint Stock Corporation (Tay Ninh, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for shrimp, published by FDA on April 27, 2011, is also listed on Import Alert 99-08 (red list), 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 listIA 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Cafatex Fishery Joint Stock Corporation
2 records, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 16-81red listShrimpSource
2009
- Import alert listingListed on Import Alert 99-08red listGreen Soybeans (Frozen) (Edamane); Soybean; Green (Frozen); Okra; FrozenSource
Questions about Cafatex Fishery Joint Stock Corporation
- Is Cafatex Fishery Joint Stock Corporation on an FDA import alert?
- Yes. As of October 26, 2026, Cafatex Fishery Joint Stock Corporation is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for shrimp; FDA published the listing on April 27, 2011.
- Has FDA refused shipments from Cafatex Fishery Joint Stock Corporation?
- No FDA import refusals for Cafatex Fishery Joint Stock Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Cafatex Fishery Joint Stock Corporation's FEI number?
- Cafatex Fishery Joint Stock Corporation's FDA Establishment Identifier (FEI) is 3004300892.
- Can shipments from Cafatex Fishery Joint Stock Corporation still enter the U.S.?
- Shipments of shrimp from Cafatex Fishery Joint Stock Corporation 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.