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Doanh Nghiep Tu Nhan Nong San Nam Ly

FDA import alert and refusal historyQuan, VietnamFEI 2000025736

Recorded by FDA as DOANH NGHIEP TU NHAN NONG SAN NAM LY

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Example subjectDoanh Nghiep Tu Nhan Nong San Nam L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Doanh Nghiep Tu Nhan Nong San Nam Ly (Quan, 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 Doanh Nghiep Tu Nhan Nong San Nam Ly

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listClams; Clams, Aquaculture Harvested Fishery/Seafood Products
    Source

Questions about Doanh Nghiep Tu Nhan Nong San Nam Ly

Is Doanh Nghiep Tu Nhan Nong San Nam Ly on an FDA import alert?
Yes. As of October 26, 2026, Doanh Nghiep Tu Nhan Nong San Nam Ly 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 Doanh Nghiep Tu Nhan Nong San Nam Ly?
No FDA import refusals for Doanh Nghiep Tu Nhan Nong San Nam Ly appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Doanh Nghiep Tu Nhan Nong San Nam Ly's FEI number?
Doanh Nghiep Tu Nhan Nong San Nam Ly's FDA Establishment Identifier (FEI) is 2000025736.
Can shipments from Doanh Nghiep Tu Nhan Nong San Nam Ly still enter the U.S.?
Shipments of clams; clams, aquaculture harvested fishery/seafood products from Doanh Nghiep Tu Nhan Nong San Nam Ly 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.