Gushi Xinxin Maltose Co., Ltd.
FDA import alert and refusal historyXinyang, ChinaFEI 3008147235
Recorded by FDA as GUSHI XINXIN MALTOSE CO., LTD.
As of October 26, 2026, Gushi Xinxin Maltose Co., Ltd. (Xinyang, China) is on the red list of FDA Import Alert 36-04 (Honey and blended syrup: drug residues) for fructose (compound malt sweetener), published by FDA on August 22, 2011, 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 36-04 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Gushi Xinxin Maltose Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 36-04red listFructose (Compound Malt Sweetener)Source
Questions about Gushi Xinxin Maltose Co., Ltd.
- Is Gushi Xinxin Maltose Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Gushi Xinxin Maltose Co., Ltd. is on the red list of FDA Import Alert 36-04, “Honey and blended syrup: drug residues”, for fructose (compound malt sweetener); FDA published the listing on August 22, 2011.
- Has FDA refused shipments from Gushi Xinxin Maltose Co., Ltd.?
- No FDA import refusals for Gushi Xinxin Maltose Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Gushi Xinxin Maltose Co., Ltd.'s FEI number?
- Gushi Xinxin Maltose Co., Ltd.'s FDA Establishment Identifier (FEI) is 3008147235.
- Can shipments from Gushi Xinxin Maltose Co., Ltd. still enter the U.S.?
- Shipments of fructose (compound malt sweetener) from Gushi Xinxin Maltose Co., Ltd. can be detained without physical examination under Import Alert 36-04; 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).
Buying from Gushi Xinxin Maltose Co., Ltd.?
Watch it and get the FDA record the day it changes. Free for one supplier.
SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.