Rodolfi Mansueto S.p.A.
FDA import alert and refusal historyCollecchio, ItalyFEI 3009942945
As of October 26, 2026, Rodolfi Mansueto S.p.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 17, 2024, 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 Rodolfi Mansueto S.p.A.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Rodolfi Mansueto S.p.A.
- Is Rodolfi Mansueto S.p.A. on an FDA import alert?
- No listing for Rodolfi Mansueto S.p.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Italy page.
- Has FDA refused shipments from Rodolfi Mansueto S.p.A.?
- No FDA import refusals for Rodolfi Mansueto S.p.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Rodolfi Mansueto S.p.A. last inspected by FDA?
- FDA's most recent inspection of Rodolfi Mansueto S.p.A. with a final classification is dated September 17, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Rodolfi Mansueto S.p.A.'s FEI number?
- Rodolfi Mansueto S.p.A.'s FDA Establishment Identifier (FEI) is 3009942945.
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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.