La Gentile S.R.L.
FDA import alert and refusal historyCortemilia, ItalyFEI 1000180928
As of October 26, 2026, La Gentile S.R.L. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 14, 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 La Gentile S.R.L.
2 records, newest first. Each line links to the FDA page it came from.
Questions about La Gentile S.R.L.
- Is La Gentile S.R.L. on an FDA import alert?
- No listing for La Gentile S.R.L. 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 La Gentile S.R.L.?
- No FDA import refusals for La Gentile S.R.L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was La Gentile S.R.L. last inspected by FDA?
- FDA's most recent inspection of La Gentile S.R.L. with a final classification is dated September 14, 2017 and was classified NAI (No Action Indicated).
- What is La Gentile S.R.L.'s FEI number?
- La Gentile S.R.L.'s FDA Establishment Identifier (FEI) is 1000180928.
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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.