Seko Sp. z o.o.
FDA import alert and refusal historyChojnice, PolandFEI 3004826726
As of October 26, 2026, Seko Sp. z o.o. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 28, 2020, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)
Every FDA record for Seko Sp. z o.o.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Seko Sp. z o.o.
- Is Seko Sp. z o.o. on an FDA import alert?
- No listing for Seko 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 Seko Sp. z o.o.?
- No FDA import refusals for Seko Sp. z o.o. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Seko Sp. z o.o. last inspected by FDA?
- FDA's most recent inspection of Seko Sp. z o.o. with a final classification is dated January 28, 2020 and was classified VAI (Voluntary Action Indicated).
- What is Seko Sp. z o.o.'s FEI number?
- Seko Sp. z o.o.'s FDA Establishment Identifier (FEI) is 3004826726.
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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.