Okregowa Spoldzielnia Mleczarska w Piatnicy
FDA import alert and refusal historyPiatnica, PolandFEI 3010011830
As of October 27, 2026, Okregowa Spoldzielnia Mleczarska w Piatnicy is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on July 20, 2026, most often for std qualit (STD QUALIT).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cream, sour · STD QUALIT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Okregowa Spoldzielnia Mleczarska w Piatnicy
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 2 lines in one entry: Cream, sour; Yogurt (plain, flavored or fruit added)STD QUALITEntry 274-2601823-3Show 2 linesHide lines
- Refused, Cream, sourSTD QUALITEntry 274-2601823-3Source
- Refused, Yogurt (plain, flavored or fruit added)STD QUALITEntry 274-2601823-3Source
Refusal charges, in plain English
- STD QUALIT2 refused lines
STD QUALIT
Questions about Okregowa Spoldzielnia Mleczarska w Piatnicy
- Is Okregowa Spoldzielnia Mleczarska w Piatnicy on an FDA import alert?
- No listing for Okregowa Spoldzielnia Mleczarska w Piatnicy appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Poland page.
- Has FDA refused shipments from Okregowa Spoldzielnia Mleczarska w Piatnicy?
- Yes. FDA refused 2 shipment lines from Okregowa Spoldzielnia Mleczarska w Piatnicy on July 20, 2026. The most recent, on July 20, 2026, was cream, sour, charged as STD QUALIT (std qualit).
- Why did FDA refuse Okregowa Spoldzielnia Mleczarska w Piatnicy's shipments?
- The most frequent charge is STD QUALIT (std qualit, 2 lines).
- What is Okregowa Spoldzielnia Mleczarska w Piatnicy's FEI number?
- Okregowa Spoldzielnia Mleczarska w Piatnicy's FDA Establishment Identifier (FEI) is 3010011830.
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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.