Vifaco Nong Hai San-Xay
FDA import alert and refusal historyHo Chi Minh City, VietnamFEI 3003526623
As of October 26, 2026, Vifaco Nong Hai San-Xay (Ho Chi Minh City, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for frozen crabmeat; shrimp; frog legs; snails, aquatic, other aquatic species; snails, terrestrial (e.g., land), other aquatic species, 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 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Vifaco Nong Hai San-Xay
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listFrozen Crabmeat; Shrimp; Frog Legs; Snails, Aquatic, Other Aquatic Species; Snails, terrestrial (e.g., land), Other Aquatic SpeciesSource
Questions about Vifaco Nong Hai San-Xay
- Is Vifaco Nong Hai San-Xay on an FDA import alert?
- Yes. As of October 26, 2026, Vifaco Nong Hai San-Xay is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for frozen crabmeat; shrimp; frog legs; snails, aquatic, other aquatic species; snails, terrestrial (e.g., land), other aquatic species; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Vifaco Nong Hai San-Xay?
- No FDA import refusals for Vifaco Nong Hai San-Xay appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Vifaco Nong Hai San-Xay's FEI number?
- Vifaco Nong Hai San-Xay's FDA Establishment Identifier (FEI) is 3003526623.
- Can shipments from Vifaco Nong Hai San-Xay still enter the U.S.?
- Shipments of frozen crabmeat; shrimp; frog legs; snails, aquatic, other aquatic species; snails, terrestrial (e.g., land), other aquatic species from Vifaco Nong Hai San-Xay 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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