Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti
FDA import alert and refusal historyManisa, TurkeyFEI 3004293909
As of October 26, 2026, Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti (Manisa, Turkey) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for stuffed vine leaves, published by FDA on May 6, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti
1 record, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 99-08red listStuffed Vine LeavesSource
Questions about Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti
- Is Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti on an FDA import alert?
- Yes. As of October 26, 2026, Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for stuffed vine leaves; FDA published the listing on May 6, 2010.
- Has FDA refused shipments from Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti?
- No FDA import refusals for Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti's FEI number?
- Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti's FDA Establishment Identifier (FEI) is 3004293909.
- Can shipments from Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti still enter the U.S.?
- Shipments of stuffed vine leaves from Herko Gida ve Mak. San. Ith. Ihr. Ltd. Sti can be detained without physical examination under Import Alert 99-08; 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.