Kauko Metex Spzo
FDA import alert and refusal historyWarsaw, PolandFEI 3003609288
As of October 26, 2026, Kauko Metex Spzo (Warsaw, Poland) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for strawberries (berry), raw - fresh, frozen, natural state; strawberries (berry), packaged food (not commercially sterile), 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kauko Metex Spzo
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listStrawberries (Berry), Raw - Fresh, Frozen, Natural State; Strawberries (Berry), Packaged Food (Not Commercially Sterile)Source
Questions about Kauko Metex Spzo
- Is Kauko Metex Spzo on an FDA import alert?
- Yes. As of October 26, 2026, Kauko Metex Spzo is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for strawberries (berry), raw - fresh, frozen, natural state; strawberries (berry), packaged food (not commercially sterile); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Kauko Metex Spzo?
- No FDA import refusals for Kauko Metex Spzo appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kauko Metex Spzo's FEI number?
- Kauko Metex Spzo's FDA Establishment Identifier (FEI) is 3003609288.
- Can shipments from Kauko Metex Spzo still enter the U.S.?
- Shipments of strawberries (berry), raw - fresh, frozen, natural state; strawberries (berry), packaged food (not commercially sterile) from Kauko Metex Spzo 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.