Gosheng Industrial (Shenzhen) Co Ltd
FDA import alert and refusal historyShenzhen, ChinaFEI 3004342414
Recorded by FDA as GOSHENG INDUSTRIAL (SHENZHEN) CO LTD
As of October 26, 2026, Gosheng Industrial (Shenzhen) Co Ltd (Shenzhen, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for fructus lycii lycium barbarum wolfberry or goji berry; ginseng powder; ginseng powder, published by FDA on September 16, 2009, 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 Gosheng Industrial (Shenzhen) Co Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listFructus Lycii Lycium Barbarum Wolfberry or Goji Berry; Ginseng powder; ginseng powderSource
Questions about Gosheng Industrial (Shenzhen) Co Ltd
- Is Gosheng Industrial (Shenzhen) Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Gosheng Industrial (Shenzhen) Co Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for fructus lycii lycium barbarum wolfberry or goji berry; ginseng powder; ginseng powder; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Gosheng Industrial (Shenzhen) Co Ltd?
- No FDA import refusals for Gosheng Industrial (Shenzhen) Co Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Gosheng Industrial (Shenzhen) Co Ltd's FEI number?
- Gosheng Industrial (Shenzhen) Co Ltd's FDA Establishment Identifier (FEI) is 3004342414.
- Can shipments from Gosheng Industrial (Shenzhen) Co Ltd still enter the U.S.?
- Shipments of fructus lycii lycium barbarum wolfberry or goji berry; ginseng powder; ginseng powder from Gosheng Industrial (Shenzhen) 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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