Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias)
FDA import alert and refusal historyHo Chi Minh City, VietnamFEI 3001783563
As of October 26, 2026, Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias) (Ho Chi Minh City, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for snake head; snakehead, 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 Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias)
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listSnake Head; SnakeheadSource
Questions about Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias)
- Is Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias) on an FDA import alert?
- Yes. As of October 26, 2026, Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias) is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for snake head; snakehead; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias)?
- No FDA import refusals for Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias)'s FEI number?
- Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias)'s FDA Establishment Identifier (FEI) is 3001783563.
- Can shipments from Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias) still enter the U.S.?
- Shipments of snake head; snakehead from Cong Ty San Xuat Va Kinh Doanh Zuat Nhap (see firm alias) 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.