Spiceland Sirafim & Co.
FDA import alert and refusal historyBelbies, EgyptFEI 3008787119
As of October 26, 2026, Spiceland Sirafim & Co. (Belbies, Egypt) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for molokhia leaves; parsley; marjoram, published by FDA on August 26, 2011, 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 Spiceland Sirafim & Co.
2 records, newest first. Each line links to the FDA page it came from.
2012
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 99-19red listMolokhia Leaves; Parsley; MarjoramSource
Questions about Spiceland Sirafim & Co.
- Is Spiceland Sirafim & Co. on an FDA import alert?
- Yes. As of October 26, 2026, Spiceland Sirafim & Co. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for molokhia leaves; parsley; marjoram; FDA published the listing on August 26, 2011.
- Has FDA refused shipments from Spiceland Sirafim & Co.?
- No FDA import refusals for Spiceland Sirafim & Co. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Spiceland Sirafim & Co. last inspected by FDA?
- FDA's most recent inspection of Spiceland Sirafim & Co. with a final classification is dated September 10, 2012 and was classified NAI (No Action Indicated).
- What is Spiceland Sirafim & Co.'s FEI number?
- Spiceland Sirafim & Co.'s FDA Establishment Identifier (FEI) is 3008787119.
- Can shipments from Spiceland Sirafim & Co. still enter the U.S.?
- Shipments of molokhia leaves; parsley; marjoram from Spiceland Sirafim & Co. 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.