Thanh Hao Seafood Co., Ltd
FDA import alert and refusal historyDat Do District, VietnamFEI 3015127411
As of October 26, 2026, Thanh Hao Seafood Co., Ltd (Dat Do District, Vietnam) is on the red list of FDA Import Alert 99-47 (Foods that appear adulterated for economic gain) for squid, published by FDA on April 2, 2024, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-47 · red list
- Last import refusal
- Squid, other aquatic species · ADDED BULK
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Thanh Hao Seafood Co., Ltd
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-47red listSquidSource
2023
- Import refusalRefused, Squid, other aquatic speciesADDED BULKEntry FY1-4027761-4Source
Refusal charges, in plain English
- ADDED BULK1 refused line
ADDED BULK
Questions about Thanh Hao Seafood Co., Ltd
- Is Thanh Hao Seafood Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Thanh Hao Seafood Co., Ltd is on the red list of FDA Import Alert 99-47, “Foods that appear adulterated for economic gain”, for squid; FDA published the listing on April 2, 2024.
- Has FDA refused shipments from Thanh Hao Seafood Co., Ltd?
- Yes. FDA refused 1 shipment line from Thanh Hao Seafood Co., Ltd on December 26, 2023. The most recent, on December 26, 2023, was squid, other aquatic species, charged as ADDED BULK (added bulk).
- Why did FDA refuse Thanh Hao Seafood Co., Ltd's shipments?
- The most frequent charge is ADDED BULK (added bulk, 1 line).
- What is Thanh Hao Seafood Co., Ltd's FEI number?
- Thanh Hao Seafood Co., Ltd's FDA Establishment Identifier (FEI) is 3015127411.
- Can shipments from Thanh Hao Seafood Co., Ltd still enter the U.S.?
- Shipments of squid from Thanh Hao Seafood Co., Ltd can be detained without physical examination under Import Alert 99-47; 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.