Kerry Polska Sp. Z O.O.
FDA import alert and refusal historyKielce, PolandFEI 3003009285
As of October 26, 2026, Kerry Polska Sp. Z O.O. (Kielce, Poland) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for cherry fruit (pit fruit), raw - fresh, frozen, natural state; cherry fruit (pit fruit), 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 Kerry Polska Sp. Z O.O.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listCherry Fruit (Pit Fruit), Raw - Fresh, Frozen, Natural State; Cherry Fruit (Pit Fruit), Packaged Food (Not Commercially Sterile)Source
Questions about Kerry Polska Sp. Z O.O.
- Is Kerry Polska Sp. Z O.O. on an FDA import alert?
- Yes. As of October 26, 2026, Kerry Polska Sp. Z O.O. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for cherry fruit (pit fruit), raw - fresh, frozen, natural state; cherry fruit (pit fruit), packaged food (not commercially sterile); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Kerry Polska Sp. Z O.O.?
- No FDA import refusals for Kerry Polska Sp. Z O.O. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kerry Polska Sp. Z O.O.'s FEI number?
- Kerry Polska Sp. Z O.O.'s FDA Establishment Identifier (FEI) is 3003009285.
- Can shipments from Kerry Polska Sp. Z O.O. still enter the U.S.?
- Shipments of cherry fruit (pit fruit), raw - fresh, frozen, natural state; cherry fruit (pit fruit), packaged food (not commercially sterile) from Kerry Polska Sp. Z O.O. 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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