S.A.Franzeluta LTD
FDA import alert and refusal historyChisinau, MoldovaFEI 3009484297
As of October 26, 2026, S.A.Franzeluta LTD (Chisinau, Moldova) is on the red list of FDA Import Alert 36-04 (Honey and blended syrup: drug residues) for honey, published by FDA on February 3, 2014, is also listed on 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
- Import alerts
- IA 36-04 · red listIA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for S.A.Franzeluta LTD
3 records, newest first. Each line links to the FDA page it came from.
2014
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 36-04red listHoneySource
2012
- Import alert listingListed on Import Alert 45-02red listGingerbread with Blackberry FlavorSource
Questions about S.A.Franzeluta LTD
- Is S.A.Franzeluta LTD on an FDA import alert?
- Yes. As of October 26, 2026, S.A.Franzeluta LTD is on the red list of FDA Import Alert 36-04, “Honey and blended syrup: drug residues”, for honey; FDA published the listing on February 3, 2014.
- Has FDA refused shipments from S.A.Franzeluta LTD?
- No FDA import refusals for S.A.Franzeluta LTD appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was S.A.Franzeluta LTD last inspected by FDA?
- FDA's most recent inspection of S.A.Franzeluta LTD with a final classification is dated July 1, 2014 and was classified NAI (No Action Indicated).
- What is S.A.Franzeluta LTD's FEI number?
- S.A.Franzeluta LTD's FDA Establishment Identifier (FEI) is 3009484297.
- Can shipments from S.A.Franzeluta LTD still enter the U.S.?
- Shipments of honey from S.A.Franzeluta LTD can be detained without physical examination under Import Alert 36-04; 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.