Newco Enterprise Inc.
FDA import alert and refusal historyCalgary, CanadaFEI 3006608128
As of October 26, 2026, Newco Enterprise Inc. (Calgary, Canada) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for brocco gen 10 sulforaphane glucosinolate capsules dietary supplements, 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
- None on record
Every FDA record for Newco Enterprise Inc.
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listBrocco Gen 10 Sulforaphane Glucosinolate Capsules Dietary SupplementsSource
Questions about Newco Enterprise Inc.
- Is Newco Enterprise Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Newco Enterprise Inc. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for brocco gen 10 sulforaphane glucosinolate capsules dietary supplements; FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Newco Enterprise Inc.?
- No FDA import refusals for Newco Enterprise Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Newco Enterprise Inc.'s FEI number?
- Newco Enterprise Inc.'s FDA Establishment Identifier (FEI) is 3006608128.
- Can shipments from Newco Enterprise Inc. still enter the U.S.?
- Shipments of brocco gen 10 sulforaphane glucosinolate capsules dietary supplements from Newco Enterprise 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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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.