Dong Guan City Howli Sheng Lian Haiwei Business Department
FDA import alert and refusal historyDong Guan City, ChinaFEI 3009870430
As of October 27, 2026, Dong Guan City Howli Sheng Lian Haiwei Business Department (Dong Guan City, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for fructus lycii, published by FDA on December 23, 2014, 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 Dong Guan City Howli Sheng Lian Haiwei Business Department
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-08red listFructus LyciiSource
Questions about Dong Guan City Howli Sheng Lian Haiwei Business Department
- Is Dong Guan City Howli Sheng Lian Haiwei Business Department on an FDA import alert?
- Yes. As of October 27, 2026, Dong Guan City Howli Sheng Lian Haiwei Business Department is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for fructus lycii; FDA published the listing on December 23, 2014.
- Has FDA refused shipments from Dong Guan City Howli Sheng Lian Haiwei Business Department?
- No FDA import refusals for Dong Guan City Howli Sheng Lian Haiwei Business Department appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Dong Guan City Howli Sheng Lian Haiwei Business Department's FEI number?
- Dong Guan City Howli Sheng Lian Haiwei Business Department's FDA Establishment Identifier (FEI) is 3009870430.
- Can shipments from Dong Guan City Howli Sheng Lian Haiwei Business Department still enter the U.S.?
- Shipments of fructus lycii from Dong Guan City Howli Sheng Lian Haiwei Business Department 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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