Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti
FDA import alert and refusal historyIzmir, TurkeyFEI 3003245971
As of October 26, 2026, Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti (Izmir, Turkey) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for cumin, ground, cracked (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 Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listCumin, Ground, Cracked (Spice)Source
Questions about Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti
- Is Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti on an FDA import alert?
- Yes. As of October 26, 2026, Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for cumin, ground, cracked (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti?
- No FDA import refusals for Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti's FEI number?
- Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti's FDA Establishment Identifier (FEI) is 3003245971.
- Can shipments from Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti still enter the U.S.?
- Shipments of cumin, ground, cracked (spice) from Herba Gida Maddeleri Ithalat Ihracat San. Ve Tic. Ldt.Sti 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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