Jilin Province Yangtianzheng Special Local Products Co.Ltd.
FDA import alert and refusal historyBaishan, ChinaFEI 3015256306
Recorded by FDA as JILIN PROVINCE YANGTIANZHENG SPECIAL LOCAL PRODUCTS CO.LTD.
As of October 27, 2026, Jilin Province Yangtianzheng Special Local Products Co.Ltd. (Baishan, China) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for astragali radix, published by FDA on July 17, 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
- None on record
Every FDA record for Jilin Province Yangtianzheng Special Local Products Co.Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-39red listAstragali radixSource
Questions about Jilin Province Yangtianzheng Special Local Products Co.Ltd.
- Is Jilin Province Yangtianzheng Special Local Products Co.Ltd. on an FDA import alert?
- Yes. As of October 27, 2026, Jilin Province Yangtianzheng Special Local Products Co.Ltd. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for astragali radix; FDA published the listing on July 17, 2024.
- Has FDA refused shipments from Jilin Province Yangtianzheng Special Local Products Co.Ltd.?
- No FDA import refusals for Jilin Province Yangtianzheng Special Local Products Co.Ltd. appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Jilin Province Yangtianzheng Special Local Products Co.Ltd.'s FEI number?
- Jilin Province Yangtianzheng Special Local Products Co.Ltd.'s FDA Establishment Identifier (FEI) is 3015256306.
- Can shipments from Jilin Province Yangtianzheng Special Local Products Co.Ltd. still enter the U.S.?
- Shipments of astragali radix from Jilin Province Yangtianzheng Special Local Products Co.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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