Qinghai Golden Desert Agricultural Development Co., Ltd.
FDA import alert and refusal historyXining, ChinaFEI 3011412553
As of October 26, 2026, Qinghai Golden Desert Agricultural Development Co., Ltd. (Xining, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for goji berries (dried wolfberries), published by FDA on June 17, 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 Qinghai Golden Desert Agricultural 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 listGoji Berries (Dried Wolfberries)Source
Questions about Qinghai Golden Desert Agricultural Development Co., Ltd.
- Is Qinghai Golden Desert Agricultural Development Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Qinghai Golden Desert Agricultural Development Co., Ltd. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for goji berries (dried wolfberries); FDA published the listing on June 17, 2015.
- Has FDA refused shipments from Qinghai Golden Desert Agricultural Development Co., Ltd.?
- No FDA import refusals for Qinghai Golden Desert Agricultural Development Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Qinghai Golden Desert Agricultural Development Co., Ltd.'s FEI number?
- Qinghai Golden Desert Agricultural Development Co., Ltd.'s FDA Establishment Identifier (FEI) is 3011412553.
- Can shipments from Qinghai Golden Desert Agricultural Development Co., Ltd. still enter the U.S.?
- Shipments of goji berries (dried wolfberries) from Qinghai Golden Desert Agricultural 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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