Georgalos Hnos.S.A.I.C.A.
FDA import alert and refusal historyRio Segundo, ArgentinaFEI 3004351899
As of October 26, 2026, Georgalos Hnos.S.A.I.C.A. (Rio Segundo, Argentina) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for nucrem peanut candy bar with sunflower and honey, published by FDA on November 18, 2015, 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 99-19 · 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 Georgalos Hnos.S.A.I.C.A.
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-19red listNucrem Peanut Candy Bar with Sunflower and HoneySource
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Questions about Georgalos Hnos.S.A.I.C.A.
- Is Georgalos Hnos.S.A.I.C.A. on an FDA import alert?
- Yes. As of October 26, 2026, Georgalos Hnos.S.A.I.C.A. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for nucrem peanut candy bar with sunflower and honey; FDA published the listing on November 18, 2015.
- Has FDA refused shipments from Georgalos Hnos.S.A.I.C.A.?
- No FDA import refusals for Georgalos Hnos.S.A.I.C.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Georgalos Hnos.S.A.I.C.A. last inspected by FDA?
- FDA's most recent inspection of Georgalos Hnos.S.A.I.C.A. with a final classification is dated May 11, 2015 and was classified NAI (No Action Indicated).
- What is Georgalos Hnos.S.A.I.C.A.'s FEI number?
- Georgalos Hnos.S.A.I.C.A.'s FDA Establishment Identifier (FEI) is 3004351899.
- Can shipments from Georgalos Hnos.S.A.I.C.A. still enter the U.S.?
- Shipments of nucrem peanut candy bar with sunflower and honey from Georgalos Hnos.S.A.I.C.A. can be detained without physical examination under Import Alert 99-19; 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.