Haikou Quanyong Aquatic Frozen & Process
FDA import alert and refusal historyHaikou, ChinaFEI 3004280036
Recorded by FDA as HAIKOU QUANYONG AQUATIC FROZEN & PROCESS
As of October 26, 2026, Haikou Quanyong Aquatic Frozen & Process (Haikou, China) is on the red list of FDA Import Alert 16-124 (Aquaculture seafood: unapproved drugs) for tilapia; tilapia, aquaculture harvested fishery/seafood products, published by FDA on September 16, 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 16-124 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Haikou Quanyong Aquatic Frozen & Process
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-124red listTilapia; Tilapia, Aquaculture Harvested Fishery/Seafood ProductsSource
Questions about Haikou Quanyong Aquatic Frozen & Process
- Is Haikou Quanyong Aquatic Frozen & Process on an FDA import alert?
- Yes. As of October 26, 2026, Haikou Quanyong Aquatic Frozen & Process is on the red list of FDA Import Alert 16-124, “Aquaculture seafood: unapproved drugs”, for tilapia; tilapia, aquaculture harvested fishery/seafood products; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Haikou Quanyong Aquatic Frozen & Process?
- No FDA import refusals for Haikou Quanyong Aquatic Frozen & Process appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Haikou Quanyong Aquatic Frozen & Process's FEI number?
- Haikou Quanyong Aquatic Frozen & Process's FDA Establishment Identifier (FEI) is 3004280036.
- Can shipments from Haikou Quanyong Aquatic Frozen & Process still enter the U.S.?
- Shipments of tilapia; tilapia, aquaculture harvested fishery/seafood products from Haikou Quanyong Aquatic Frozen & Process can be detained without physical examination under Import Alert 16-124; 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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