Suzhou Houssy Drinks Co., Ltd
FDA import alert and refusal historySuzhou, ChinaFEI 3007133592
As of October 27, 2026, Suzhou Houssy Drinks Co., Ltd (Suzhou, China) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for aloe vera drink; guava flavor, published by FDA on July 8, 2016, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Suzhou Houssy Drinks Co., Ltd
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 45-02red listAloe vera drink; Guava flavorSource
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Suzhou Houssy Drinks Co., Ltd
- Is Suzhou Houssy Drinks Co., Ltd on an FDA import alert?
- Yes. As of October 27, 2026, Suzhou Houssy Drinks Co., Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for aloe vera drink; guava flavor; FDA published the listing on July 8, 2016.
- Has FDA refused shipments from Suzhou Houssy Drinks Co., Ltd?
- No FDA import refusals for Suzhou Houssy Drinks Co., Ltd appear in FDA's refusal data since October 2016, as of October 27, 2026.
- When was Suzhou Houssy Drinks Co., Ltd last inspected by FDA?
- FDA's most recent inspection of Suzhou Houssy Drinks Co., Ltd with a final classification is dated May 20, 2014 and was classified VAI (Voluntary Action Indicated).
- What is Suzhou Houssy Drinks Co., Ltd's FEI number?
- Suzhou Houssy Drinks Co., Ltd's FDA Establishment Identifier (FEI) is 3007133592.
- Can shipments from Suzhou Houssy Drinks Co., Ltd still enter the U.S.?
- Shipments of aloe vera drink; guava flavor from Suzhou Houssy Drinks Co., Ltd can be detained without physical examination under Import Alert 45-02; 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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