Kazeina Polska Sp. z.o.o.
FDA import alert and refusal historyPultusk, PolandFEI 3004040439
As of October 26, 2026, Kazeina Polska Sp. z.o.o. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 30, 2018, was classified NAI (No Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Kazeina Polska Sp. z.o.o.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Kazeina Polska Sp. z.o.o.
- Is Kazeina Polska Sp. z.o.o. on an FDA import alert?
- No listing for Kazeina Polska Sp. z.o.o. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Poland page.
- Has FDA refused shipments from Kazeina Polska Sp. z.o.o.?
- No FDA import refusals for Kazeina Polska Sp. z.o.o. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Kazeina Polska Sp. z.o.o. last inspected by FDA?
- FDA's most recent inspection of Kazeina Polska Sp. z.o.o. with a final classification is dated August 30, 2018 and was classified NAI (No Action Indicated).
- What is Kazeina Polska Sp. z.o.o.'s FEI number?
- Kazeina Polska Sp. z.o.o.'s FDA Establishment Identifier (FEI) is 3004040439.
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