Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd
FDA import alert and refusal historyChengdu, ChinaFEI 3021169816
Recorded by FDA as SANJIE XINGHUA (SICHUAN) ENTERPRISE MANAGEMENT CO.,LTD
As of October 27, 2026, Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd (Chengdu, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for shiitake mushroom, published by FDA on December 2, 2022, 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 Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd
1 record, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-08red listShiitake MushroomSource
Questions about Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd
- Is Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd on an FDA import alert?
- Yes. As of October 27, 2026, Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for shiitake mushroom; FDA published the listing on December 2, 2022.
- Has FDA refused shipments from Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd?
- No FDA import refusals for Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd's FEI number?
- Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd's FDA Establishment Identifier (FEI) is 3021169816.
- Can shipments from Sanjie Xinghua (Sichuan) Enterprise Management Co.,Ltd still enter the U.S.?
- Shipments of shiitake mushroom from Sanjie Xinghua (Sichuan) Enterprise Management 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.