Creta Mel SA
FDA import alert and refusal historyRethymno, GreeceFEI 3004281785
Recorded by FDA as CRETA MEL SA
As of October 25, 2026, Creta Mel SA (Rethymno, Greece) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft nougat (dried fruits); soft nougat (strawberry), published by FDA on August 9, 2010, 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
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Creta Mel SA
2 records, newest first. Each line links to the FDA page it came from.
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 45-02red listSoft Nougat (Dried Fruits); Soft Nougat (Strawberry)Source
Questions about Creta Mel SA
- Is Creta Mel SA on an FDA import alert?
- Yes. As of October 25, 2026, Creta Mel SA is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft nougat (dried fruits); soft nougat (strawberry); FDA published the listing on August 9, 2010.
- Has FDA refused shipments from Creta Mel SA?
- No FDA import refusals for Creta Mel SA appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Creta Mel SA last inspected by FDA?
- FDA's most recent inspection of Creta Mel SA with a final classification is dated May 2, 2012 and was classified VAI (Voluntary Action Indicated).
- What is Creta Mel SA's FEI number?
- Creta Mel SA's FDA Establishment Identifier (FEI) is 3004281785.
- Can shipments from Creta Mel SA still enter the U.S.?
- Shipments of soft nougat (dried fruits); soft nougat (strawberry) from Creta Mel 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.