Neromodena
FDA import alert and refusal historyModena, ItalyFEI 3005389199
As of October 26, 2026, Neromodena has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 19, 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 Neromodena
2 records, newest first. Each line links to the FDA page it came from.
Questions about Neromodena
- Is Neromodena on an FDA import alert?
- No listing for Neromodena 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 Neromodena?
- No FDA import refusals for Neromodena appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Neromodena last inspected by FDA?
- FDA's most recent inspection of Neromodena with a final classification is dated September 19, 2024 and was classified NAI (No Action Indicated).
- What is Neromodena's FEI number?
- Neromodena's FDA Establishment Identifier (FEI) is 3005389199.
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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.