Fu-Ming International Enterprise Ltd.
FDA import alert and refusal historyKaohsiung, TaiwanFEI 3004260186
Recorded by FDA as FU-MING INTERNATIONAL ENTERPRISE LTD.
As of October 26, 2026, Fu-Ming International Enterprise Ltd. (Kaohsiung, Taiwan) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tilapia; frog legs; tilapia, 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 Fu-Ming International Enterprise Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listTilapia; Frog Legs; Tilapia, Aquaculture Harvested Fishery/Seafood ProductsSource
Questions about Fu-Ming International Enterprise Ltd.
- Is Fu-Ming International Enterprise Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Fu-Ming International Enterprise Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tilapia; frog legs; tilapia, aquaculture harvested fishery/seafood products; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Fu-Ming International Enterprise Ltd.?
- No FDA import refusals for Fu-Ming International Enterprise Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Fu-Ming International Enterprise Ltd.'s FEI number?
- Fu-Ming International Enterprise Ltd.'s FDA Establishment Identifier (FEI) is 3004260186.
- Can shipments from Fu-Ming International Enterprise Ltd. still enter the U.S.?
- Shipments of tilapia; frog legs; tilapia, aquaculture harvested fishery/seafood products from Fu-Ming International Enterprise 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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