Hochland Polska Sp. z.o.o.
FDA import alert and refusal historyKazmierz, PolandFEI 3003297917
As of October 26, 2026, Hochland 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 29, 2024, 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 Hochland Polska Sp. z.o.o.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Hochland Polska Sp. z.o.o.
- Is Hochland Polska Sp. z.o.o. on an FDA import alert?
- No listing for Hochland 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 Hochland Polska Sp. z.o.o.?
- No FDA import refusals for Hochland Polska Sp. z.o.o. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Hochland Polska Sp. z.o.o. last inspected by FDA?
- FDA's most recent inspection of Hochland Polska Sp. z.o.o. with a final classification is dated August 29, 2024 and was classified NAI (No Action Indicated).
- What is Hochland Polska Sp. z.o.o.'s FEI number?
- Hochland Polska Sp. z.o.o.'s FDA Establishment Identifier (FEI) is 3003297917.
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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.