China Sinopharm International (Shanghai) Co. Ltd
FDA import alert and refusal historyShanghai, ChinaFEI 3011650878
Recorded by FDA as CHINA SINOPHARM INTERNATIONAL (SHANGHAI) CO. LTD
As of October 27, 2026, China Sinopharm International (Shanghai) Co. Ltd (Shanghai, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for ginkgo biloba extract powder, published by FDA on January 13, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for China Sinopharm International (Shanghai) Co. Ltd
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-08red listGinkgo Biloba Extract PowderSource
Questions about China Sinopharm International (Shanghai) Co. Ltd
- Is China Sinopharm International (Shanghai) Co. Ltd on an FDA import alert?
- Yes. As of October 27, 2026, China Sinopharm International (Shanghai) Co. Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for ginkgo biloba extract powder; FDA published the listing on January 13, 2015.
- Has FDA refused shipments from China Sinopharm International (Shanghai) Co. Ltd?
- No FDA import refusals for China Sinopharm International (Shanghai) Co. Ltd appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is China Sinopharm International (Shanghai) Co. Ltd's FEI number?
- China Sinopharm International (Shanghai) Co. Ltd's FDA Establishment Identifier (FEI) is 3011650878.
- Can shipments from China Sinopharm International (Shanghai) Co. Ltd still enter the U.S.?
- Shipments of ginkgo biloba extract powder from China Sinopharm International (Shanghai) Co. Ltd can be detained without physical examination under Import Alert 99-08; 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.