Xi Xia Heng Chang Long Botanical Development Co., Ltd.
FDA import alert and refusal historyXixia County, ChinaFEI 3011438438
As of October 26, 2026, Xi Xia Heng Chang Long Botanical Development Co., Ltd. (Xixia County, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for whole dried shitake mushrooms, published by FDA on March 31, 2015, 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 Xi Xia Heng Chang Long Botanical Development Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-08red listWhole dried Shitake MushroomsSource
Questions about Xi Xia Heng Chang Long Botanical Development Co., Ltd.
- Is Xi Xia Heng Chang Long Botanical Development Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Xi Xia Heng Chang Long Botanical Development Co., Ltd. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for whole dried shitake mushrooms; FDA published the listing on March 31, 2015.
- Has FDA refused shipments from Xi Xia Heng Chang Long Botanical Development Co., Ltd.?
- No FDA import refusals for Xi Xia Heng Chang Long Botanical Development Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Xi Xia Heng Chang Long Botanical Development Co., Ltd.'s FEI number?
- Xi Xia Heng Chang Long Botanical Development Co., Ltd.'s FDA Establishment Identifier (FEI) is 3011438438.
- Can shipments from Xi Xia Heng Chang Long Botanical Development Co., Ltd. still enter the U.S.?
- Shipments of whole dried shitake mushrooms from Xi Xia Heng Chang Long Botanical Development 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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