Cernelle Sa
FDA import alert and refusal historyBarbengo, SwitzerlandFEI 3002668786
As of October 25, 2026, Cernelle Sa (Barbengo, Switzerland) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.; food supplement tablets pollisport 11/8/99, published by FDA on September 18, 2009, 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
- None on record
Every FDA record for Cernelle Sa
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listVitamin, Mineral, Proteins and Unconventional Dietary Specialities For Humans and Animals, N.E.C.; Food supplement tablets Pollisport 11/8/99Source
Questions about Cernelle Sa
- Is Cernelle Sa on an FDA import alert?
- Yes. As of October 25, 2026, Cernelle Sa is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.; food supplement tablets pollisport 11/8/99; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Cernelle Sa?
- No FDA import refusals for Cernelle Sa appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Cernelle Sa's FEI number?
- Cernelle Sa's FDA Establishment Identifier (FEI) is 3002668786.
- Can shipments from Cernelle Sa still enter the U.S.?
- Shipments of vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.; food supplement tablets pollisport 11/8/99 from Cernelle Sa 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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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.