Guangdong Qingyunshan Pharmaceutical Co.,Ltd
FDA import alert and refusal historyShaoguan, ChinaFEI 3014716927
Recorded by FDA as GUANGDONG QINGYUNSHAN PHARMACEUTICAL CO.,LTD
As of October 26, 2026, Guangdong Qingyunshan Pharmaceutical Co.,Ltd (Shaoguan, China) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for gin seng jiao rejuvenate tonic, published by FDA on March 11, 2026, 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 99-45 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Guangdong Qingyunshan Pharmaceutical Co.,Ltd
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-45red listGin seng jiao rejuvenate tonicSource
Questions about Guangdong Qingyunshan Pharmaceutical Co.,Ltd
- Is Guangdong Qingyunshan Pharmaceutical Co.,Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Guangdong Qingyunshan Pharmaceutical Co.,Ltd is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for gin seng jiao rejuvenate tonic; FDA published the listing on March 11, 2026.
- Has FDA refused shipments from Guangdong Qingyunshan Pharmaceutical Co.,Ltd?
- No FDA import refusals for Guangdong Qingyunshan Pharmaceutical Co.,Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Guangdong Qingyunshan Pharmaceutical Co.,Ltd's FEI number?
- Guangdong Qingyunshan Pharmaceutical Co.,Ltd's FDA Establishment Identifier (FEI) is 3014716927.
- Can shipments from Guangdong Qingyunshan Pharmaceutical Co.,Ltd still enter the U.S.?
- Shipments of gin seng jiao rejuvenate tonic from Guangdong Qingyunshan Pharmaceutical Co.,Ltd can be detained without physical examination under Import Alert 99-45; 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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