Weifang Hongqiao International Logistics Co.,Ltd
FDA import alert and refusal historyWeifang, ChinaFEI 3011293846
Recorded by FDA as WEIFANG HONGQIAO INTERNATIONAL LOGISTICS CO.,LTD
As of October 27, 2026, Weifang Hongqiao International Logistics Co.,Ltd (Weifang, China) is on the red list of FDA Import Alert 99-35 (Fresh produce: insanitary conditions) for enoki mushrooms, published by FDA on March 24, 2023, is also listed on Import Alert 99-23 (red list), 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 99-35 · red listIA 99-23 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Weifang Hongqiao International Logistics Co.,Ltd
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-35red listEnoki MushroomsSource
- Import alert listingListed on Import Alert 99-23red listEnoki MushroomSource
Questions about Weifang Hongqiao International Logistics Co.,Ltd
- Is Weifang Hongqiao International Logistics Co.,Ltd on an FDA import alert?
- Yes. As of October 27, 2026, Weifang Hongqiao International Logistics Co.,Ltd is on the red list of FDA Import Alert 99-35, “Fresh produce: insanitary conditions”, for enoki mushrooms; FDA published the listing on March 24, 2023.
- Has FDA refused shipments from Weifang Hongqiao International Logistics Co.,Ltd?
- No FDA import refusals for Weifang Hongqiao International Logistics Co.,Ltd appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Weifang Hongqiao International Logistics Co.,Ltd's FEI number?
- Weifang Hongqiao International Logistics Co.,Ltd's FDA Establishment Identifier (FEI) is 3011293846.
- Can shipments from Weifang Hongqiao International Logistics Co.,Ltd still enter the U.S.?
- Shipments of enoki mushrooms from Weifang Hongqiao International Logistics Co.,Ltd can be detained without physical examination under Import Alert 99-35; 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.