Pinar Sut Mam.San.A.S.
FDA import alert and refusal historyEskisehir, TurkeyFEI 3011827960
As of October 26, 2026, Pinar Sut Mam.San.A.S. (Eskisehir, Turkey) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for apple juice, published by FDA on October 14, 2022, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-42 · red list
- Last import refusal
- Apple, core fruit juices or concentrates · POISONOUS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pinar Sut Mam.San.A.S.
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-42red listApple JuiceSource
2018
Refusal charges, in plain English
- POISONOUS1 refused line
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
Questions about Pinar Sut Mam.San.A.S.
- Is Pinar Sut Mam.San.A.S. on an FDA import alert?
- Yes. As of October 26, 2026, Pinar Sut Mam.San.A.S. is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for apple juice; FDA published the listing on October 14, 2022.
- Has FDA refused shipments from Pinar Sut Mam.San.A.S.?
- Yes. FDA refused 1 shipment line from Pinar Sut Mam.San.A.S. on October 9, 2018. The most recent, on October 9, 2018, was apple, core fruit juices or concentrates, charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Pinar Sut Mam.San.A.S.'s shipments?
- The most frequent charge is POISONOUS (poisonous or deleterious substance, 1 line).
- What is Pinar Sut Mam.San.A.S.'s FEI number?
- Pinar Sut Mam.San.A.S.'s FDA Establishment Identifier (FEI) is 3011827960.
- Can shipments from Pinar Sut Mam.San.A.S. still enter the U.S.?
- Shipments of apple juice from Pinar Sut Mam.San.A.S. can be detained without physical examination under Import Alert 99-42; 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.