Soylutions Inc.
FDA import alert and refusal historyQuebec, CanadaFEI 3004681861
As of October 25, 2026, Soylutions Inc. (Quebec, Canada) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for hemp dream hemp drink; unsweetened original hemp bliss organic hemp milk, published by FDA on October 2, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Soylutions Inc.
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listHemp Dream Hemp Drink; Unsweetened Original Hemp Bliss Organic Hemp MilkSource
2010
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Soylutions Inc.
- Is Soylutions Inc. on an FDA import alert?
- Yes. As of October 25, 2026, Soylutions Inc. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for hemp dream hemp drink; unsweetened original hemp bliss organic hemp milk; FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Soylutions Inc.?
- No FDA import refusals for Soylutions Inc. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Soylutions Inc. last inspected by FDA?
- FDA's most recent inspection of Soylutions Inc. with a final classification is dated June 25, 2010 and was classified NAI (No Action Indicated).
- What is Soylutions Inc.'s FEI number?
- Soylutions Inc.'s FDA Establishment Identifier (FEI) is 3004681861.
- Can shipments from Soylutions Inc. still enter the U.S.?
- Shipments of hemp dream hemp drink; unsweetened original hemp bliss organic hemp milk from Soylutions Inc. can be detained without physical examination under Import Alert 99-39; 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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