Bai Xian Wu Enterprise Company Limited
FDA import alert and refusal historyGao Xiong Shi, TaiwanFEI 3005037091
Recorded by FDA as BAI XIAN WU ENTERPRISE COMPANY LIMITED
As of October 27, 2026, Bai Xian Wu Enterprise Company Limited (Gao Xiong Shi, Taiwan) is on the red list of FDA Import Alert 16-124 (Aquaculture seafood: unapproved drugs) for tilapia, published by FDA on November 24, 2010, is also listed on Import Alert 16-81 (red list) and Import Alert 99-08 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Bai Xian Wu Enterprise Company Limited
3 records, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 16-124red listTilapiaSource
2009
- Import alert listingListed on Import Alert 16-81red listEscolarSource
- Import alert listingListed on Import Alert 99-08red listMilkfishSource
Questions about Bai Xian Wu Enterprise Company Limited
- Is Bai Xian Wu Enterprise Company Limited on an FDA import alert?
- Yes. As of October 27, 2026, Bai Xian Wu Enterprise Company Limited is on the red list of FDA Import Alert 16-124, “Aquaculture seafood: unapproved drugs”, for tilapia; FDA published the listing on November 24, 2010.
- Has FDA refused shipments from Bai Xian Wu Enterprise Company Limited?
- No FDA import refusals for Bai Xian Wu Enterprise Company Limited appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Bai Xian Wu Enterprise Company Limited's FEI number?
- Bai Xian Wu Enterprise Company Limited's FDA Establishment Identifier (FEI) is 3005037091.
- Can shipments from Bai Xian Wu Enterprise Company Limited still enter the U.S.?
- Shipments of tilapia from Bai Xian Wu Enterprise Company Limited 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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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.