Shandong Youhe Biotechnology Co., Ltd.
FDA import alert and refusal historyJing City, ChinaFEI 3021238448
As of October 26, 2026, Shandong Youhe Biotechnology Co., Ltd. (Jing City, China) is on the red list of FDA Import Alert 99-35 (Fresh produce: insanitary conditions) for enoki mushrooms, published by FDA on November 28, 2022, 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 Shandong Youhe Biotechnology Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-35red listEnoki MushroomsSource
- Import alert listingListed on Import Alert 99-23red listEnoki MushroomsSource
Questions about Shandong Youhe Biotechnology Co., Ltd.
- Is Shandong Youhe Biotechnology Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Shandong Youhe Biotechnology 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 November 28, 2022.
- Has FDA refused shipments from Shandong Youhe Biotechnology Co., Ltd.?
- No FDA import refusals for Shandong Youhe Biotechnology Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Shandong Youhe Biotechnology Co., Ltd.'s FEI number?
- Shandong Youhe Biotechnology Co., Ltd.'s FDA Establishment Identifier (FEI) is 3021238448.
- Can shipments from Shandong Youhe Biotechnology Co., Ltd. still enter the U.S.?
- Shipments of enoki mushrooms from Shandong Youhe Biotechnology 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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