Vietnam Northern Viking Technologies Co., Ltd.
FDA import alert and refusal historyHo Chi Minh, VietnamFEI 3003318879
As of October 26, 2026, Vietnam Northern Viking Technologies Co., Ltd. (Ho Chi Minh, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for clams; clams, 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 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Vietnam Northern Viking Technologies Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listClams; Clams, Aquaculture Harvested Fishery/Seafood ProductsSource
Questions about Vietnam Northern Viking Technologies Co., Ltd.
- Is Vietnam Northern Viking Technologies Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Vietnam Northern Viking Technologies Co., Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for clams; clams, aquaculture harvested fishery/seafood products; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Vietnam Northern Viking Technologies Co., Ltd.?
- No FDA import refusals for Vietnam Northern Viking Technologies Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Vietnam Northern Viking Technologies Co., Ltd.'s FEI number?
- Vietnam Northern Viking Technologies Co., Ltd.'s FDA Establishment Identifier (FEI) is 3003318879.
- Can shipments from Vietnam Northern Viking Technologies Co., Ltd. still enter the U.S.?
- Shipments of clams; clams, aquaculture harvested fishery/seafood products from Vietnam Northern Viking Technologies 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.