Abido
FDA import alert and refusal historyBeirut, LebanonFEI 3005080390
As of October 25, 2026, Abido (Beirut, Lebanon) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for thyme mixed, published by FDA on September 19, 2012, 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
- None on record
Every FDA record for Abido
1 record, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 99-19red listThyme MixedSource
Questions about Abido
- Is Abido on an FDA import alert?
- Yes. As of October 25, 2026, Abido is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for thyme mixed; FDA published the listing on September 19, 2012.
- Has FDA refused shipments from Abido?
- No FDA import refusals for Abido appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Abido's FEI number?
- Abido's FDA Establishment Identifier (FEI) is 3005080390.
- Can shipments from Abido still enter the U.S.?
- Shipments of thyme mixed from Abido 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.