Collective enterprise "Rosinka"
FDA import alert and refusal historyKyiv, UkraineFEI 3004303303
As of October 26, 2026, Collective enterprise "Rosinka" (Kyiv, Ukraine) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for tarrafon carbonated soft drink; feijoa soft drink, 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 Collective enterprise "Rosinka"
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listTarrafon carbonated soft drink; FEIJOA soft drinkSource
Questions about Collective enterprise "Rosinka"
- Is Collective enterprise "Rosinka" on an FDA import alert?
- Yes. As of October 26, 2026, Collective enterprise "Rosinka" is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for tarrafon carbonated soft drink; feijoa soft drink; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Collective enterprise "Rosinka"?
- No FDA import refusals for Collective enterprise "Rosinka" appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Collective enterprise "Rosinka"'s FEI number?
- Collective enterprise "Rosinka"'s FDA Establishment Identifier (FEI) is 3004303303.
- Can shipments from Collective enterprise "Rosinka" still enter the U.S.?
- Shipments of tarrafon carbonated soft drink; feijoa soft drink from Collective enterprise "Rosinka" 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.