Eu Yan Sang (Hong Kong) Ltd.
FDA import alert and refusal historyYuen Long, Hong KongFEI 3004262107
As of October 26, 2026, Eu Yan Sang (Hong Kong) Ltd. (Yuen Long, Hong Kong) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for bak foong pills, published by FDA on September 27, 2024, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Eu Yan Sang (Hong Kong) Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-39red listBak Foong PillsSource
2014
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and EconSource
Questions about Eu Yan Sang (Hong Kong) Ltd.
- Is Eu Yan Sang (Hong Kong) Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Eu Yan Sang (Hong Kong) Ltd. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for bak foong pills; FDA published the listing on September 27, 2024.
- Has FDA refused shipments from Eu Yan Sang (Hong Kong) Ltd.?
- No FDA import refusals for Eu Yan Sang (Hong Kong) Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Eu Yan Sang (Hong Kong) Ltd. last inspected by FDA?
- FDA's most recent inspection of Eu Yan Sang (Hong Kong) Ltd. with a final classification is dated February 18, 2014 and was classified NAI (No Action Indicated).
- What is Eu Yan Sang (Hong Kong) Ltd.'s FEI number?
- Eu Yan Sang (Hong Kong) Ltd.'s FDA Establishment Identifier (FEI) is 3004262107.
- Can shipments from Eu Yan Sang (Hong Kong) Ltd. still enter the U.S.?
- Shipments of bak foong pills from Eu Yan Sang (Hong Kong) Ltd. can be detained without physical examination under Import Alert 99-39; 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.