Salloum Bros Industry & trading SARL
FDA import alert and refusal historySelaata, LebanonFEI 3009986952
As of October 27, 2026, Salloum Bros Industry & trading SARL (Selaata, Lebanon) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for marjoram, whole (spice); marjoram, ground, cracked (spice); marjoram, natural extract or flavor (spice), published by FDA on September 16, 2009, 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 Salloum Bros Industry & trading SARL
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listMarjoram, Whole (Spice); Marjoram, Ground, Cracked (Spice); Marjoram, Natural Extract or Flavor (Spice)Source
Questions about Salloum Bros Industry & trading SARL
- Is Salloum Bros Industry & trading SARL on an FDA import alert?
- Yes. As of October 27, 2026, Salloum Bros Industry & trading SARL is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for marjoram, whole (spice); marjoram, ground, cracked (spice); marjoram, natural extract or flavor (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Salloum Bros Industry & trading SARL?
- No FDA import refusals for Salloum Bros Industry & trading SARL appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Salloum Bros Industry & trading SARL's FEI number?
- Salloum Bros Industry & trading SARL's FDA Establishment Identifier (FEI) is 3009986952.
- Can shipments from Salloum Bros Industry & trading SARL still enter the U.S.?
- Shipments of marjoram, whole (spice); marjoram, ground, cracked (spice); marjoram, natural extract or flavor (spice) from Salloum Bros Industry & trading SARL 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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