Runoland Sp. z.o.o. - Sp. J.
FDA import alert and refusal historyGora, PolandFEI 3003781517
As of October 26, 2026, Runoland Sp. z.o.o. - Sp. J. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 31, 2017, 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 Runoland Sp. z.o.o. - Sp. J.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Runoland Sp. z.o.o. - Sp. J.
- Is Runoland Sp. z.o.o. - Sp. J. on an FDA import alert?
- No listing for Runoland Sp. z.o.o. - Sp. J. 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 Runoland Sp. z.o.o. - Sp. J.?
- No FDA import refusals for Runoland Sp. z.o.o. - Sp. J. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Runoland Sp. z.o.o. - Sp. J. last inspected by FDA?
- FDA's most recent inspection of Runoland Sp. z.o.o. - Sp. J. with a final classification is dated January 31, 2017 and was classified NAI (No Action Indicated).
- What is Runoland Sp. z.o.o. - Sp. J.'s FEI number?
- Runoland Sp. z.o.o. - Sp. J.'s FDA Establishment Identifier (FEI) is 3003781517.
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