Beijing Jianyang Health Product Co., Ltd
FDA import alert and refusal historyBeijing, ChinaFEI 2000025150
Recorded by FDA as BEIJING JIANYANG HEALTH PRODUCT CO., LTD
As of October 26, 2026, Beijing Jianyang Health Product Co., Ltd (Beijing, China) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for super shanghai strong testis capsules "dietary supplement", published by FDA on May 7, 2015, 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 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Beijing Jianyang Health Product Co., Ltd
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 54-16red listSuper Shanghai Strong Testis Capsules "Dietary Supplement"Source
Questions about Beijing Jianyang Health Product Co., Ltd
- Is Beijing Jianyang Health Product Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Beijing Jianyang Health Product Co., Ltd is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for super shanghai strong testis capsules "dietary supplement"; FDA published the listing on May 7, 2015.
- Has FDA refused shipments from Beijing Jianyang Health Product Co., Ltd?
- No FDA import refusals for Beijing Jianyang Health Product Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Beijing Jianyang Health Product Co., Ltd's FEI number?
- Beijing Jianyang Health Product Co., Ltd's FDA Establishment Identifier (FEI) is 2000025150.
- Can shipments from Beijing Jianyang Health Product Co., Ltd still enter the U.S.?
- Shipments of super shanghai strong testis capsules "dietary supplement" from Beijing Jianyang Health Product Co., Ltd can be detained without physical examination under Import Alert 54-16; 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.