Lebanese Company for Modern Food Industries s.a.r.l
FDA import alert and refusal historyZahleh El Midan, LebanonFEI 3007167771
As of October 27, 2026, Lebanese Company for Modern Food Industries s.a.r.l (Zahleh El Midan, Lebanon) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for pepper; black ground; cracked; ground cumin, published by FDA on August 14, 2010, 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 Lebanese Company for Modern Food Industries s.a.r.l
1 record, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 99-19red listPepper; Black Ground; Cracked; Ground CuminSource
Questions about Lebanese Company for Modern Food Industries s.a.r.l
- Is Lebanese Company for Modern Food Industries s.a.r.l on an FDA import alert?
- Yes. As of October 27, 2026, Lebanese Company for Modern Food Industries s.a.r.l is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for pepper; black ground; cracked; ground cumin; FDA published the listing on August 14, 2010.
- Has FDA refused shipments from Lebanese Company for Modern Food Industries s.a.r.l?
- No FDA import refusals for Lebanese Company for Modern Food Industries s.a.r.l appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Lebanese Company for Modern Food Industries s.a.r.l's FEI number?
- Lebanese Company for Modern Food Industries s.a.r.l's FDA Establishment Identifier (FEI) is 3007167771.
- Can shipments from Lebanese Company for Modern Food Industries s.a.r.l still enter the U.S.?
- Shipments of pepper; black ground; cracked; ground cumin from Lebanese Company for Modern Food Industries s.a.r.l 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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