Quanto Mais Import and Export
FDA import alert and refusal historyRio De Janeiro, BrazilFEI 3004658172
As of October 26, 2026, Quanto Mais Import and Export (Rio De Janeiro, Brazil) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for tang maracuja fruit juice drinks, published by FDA on May 13, 2025, is also listed on Import Alert 99-39 (red list) and Import Alert 45-02 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Quanto Mais Import and Export
3 records, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 99-45red listTang Maracuja Fruit Juice DrinksSource
- Import alert listingListed on Import Alert 99-39red listTang Maracuja Fruit Juice DrinksSource
2011
- Import alert listingListed on Import Alert 45-02red listTang Maracuja Passionfruit; Grosselhacamp Flavoring; Uvacamp Flavoring Grape ConcentrateSource
Questions about Quanto Mais Import and Export
- Is Quanto Mais Import and Export on an FDA import alert?
- Yes. As of October 26, 2026, Quanto Mais Import and Export is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for tang maracuja fruit juice drinks; FDA published the listing on May 13, 2025.
- Has FDA refused shipments from Quanto Mais Import and Export?
- No FDA import refusals for Quanto Mais Import and Export appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Quanto Mais Import and Export's FEI number?
- Quanto Mais Import and Export's FDA Establishment Identifier (FEI) is 3004658172.
- Can shipments from Quanto Mais Import and Export still enter the U.S.?
- Shipments of tang maracuja fruit juice drinks from Quanto Mais Import and Export can be detained without physical examination under Import Alert 99-45; 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.