Medi Ozel Gida Sanayi ve Ticaret A.S
FDA import alert and refusal historyIzmir, TurkeyFEI 3004796004
As of October 26, 2026, Medi Ozel Gida Sanayi ve Ticaret A.S (Izmir, Turkey) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for sundried tomato halves, published by FDA on September 15, 2013, 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 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Medi Ozel Gida Sanayi ve Ticaret A.S
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 99-21red listSundried Tomato HalvesSource
Questions about Medi Ozel Gida Sanayi ve Ticaret A.S
- Is Medi Ozel Gida Sanayi ve Ticaret A.S on an FDA import alert?
- Yes. As of October 26, 2026, Medi Ozel Gida Sanayi ve Ticaret A.S is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for sundried tomato halves; FDA published the listing on September 15, 2013.
- Has FDA refused shipments from Medi Ozel Gida Sanayi ve Ticaret A.S?
- No FDA import refusals for Medi Ozel Gida Sanayi ve Ticaret A.S appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Medi Ozel Gida Sanayi ve Ticaret A.S's FEI number?
- Medi Ozel Gida Sanayi ve Ticaret A.S's FDA Establishment Identifier (FEI) is 3004796004.
- Can shipments from Medi Ozel Gida Sanayi ve Ticaret A.S still enter the U.S.?
- Shipments of sundried tomato halves from Medi Ozel Gida Sanayi ve Ticaret A.S can be detained without physical examination under Import Alert 99-21; 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.