Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh
FDA import alert and refusal historyCam Lam, VietnamFEI 3013007581
Recorded by FDA as THONG THUAN - CAM RANH SEAFOOD JOINT STOCK COMPANY - EXPORT SEAFOOD PROCESSING FACTORY - CAM RANH
As of October 26, 2026, Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh (Cam Lam, Vietnam) is on the red list of FDA Import Alert 16-129 (Seafood products: nitrofurans) for shrimp, published by FDA on May 8, 2025, is also listed on Import Alert 16-124 (red list) and Import Alert 16-127 (red list), and has 4 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- Shrimp and prawns, aquaculture harvested fishery/seafood products · NITROFURAN
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh
7 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 082-0461002-9Source
- Import alert listingListed on Import Alert 16-129red listShrimpSource
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsPOIS CHLOREntry 082-0461806-3Source
- Import alert listingListed on Import Alert 16-124red listShrimpSource
- Import alert listingListed on Import Alert 16-127red listShrimpSource
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 082-0458781-3Source
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 082-0458781-3Source
Refusal charges, in plain English
- VETDRUGRES2 refused lines
Animal drug residue
The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.
- NITROFURAN1 refused line
Nitrofurans
The product appeared to contain nitrofurans, a class of antibiotic drugs, which are treated as an unsafe food additive under section 409 of the FD&C Act.
- POIS CHLOR1 refused line
POIS CHLOR
Questions about Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh
- Is Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh on an FDA import alert?
- Yes. As of October 26, 2026, Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh is on the red list of FDA Import Alert 16-129, “Seafood products: nitrofurans”, for shrimp; FDA published the listing on May 8, 2025.
- Has FDA refused shipments from Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh?
- Yes. FDA refused 4 shipment lines from Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh between February 28, 2025 and May 27, 2025. The most recent, on May 27, 2025, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as NITROFURAN (nitrofurans).
- Why did FDA refuse Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh's shipments?
- The most frequent charges are VETDRUGRES (animal drug residue, 2 lines) and NITROFURAN (nitrofurans, 1 line).
- What is Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh's FEI number?
- Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh's FDA Establishment Identifier (FEI) is 3013007581.
- Can shipments from Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh still enter the U.S.?
- Shipments of shrimp from Thong Thuan - Cam Ranh Seafood Joint Stock Company - Export Seafood Processing Factory - Cam Ranh can be detained without physical examination under Import Alert 16-129; 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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