Lunor
FDA import alert and refusal historyLuneray, FranceFEI 3003002329
As of October 26, 2026, Lunor has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 12, 2018, 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 Lunor
2 records, newest first. Each line links to the FDA page it came from.
Questions about Lunor
- Is Lunor on an FDA import alert?
- No listing for Lunor appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
- Has FDA refused shipments from Lunor?
- No FDA import refusals for Lunor appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Lunor last inspected by FDA?
- FDA's most recent inspection of Lunor with a final classification is dated June 12, 2018 and was classified NAI (No Action Indicated).
- What is Lunor's FEI number?
- Lunor's FDA Establishment Identifier (FEI) is 3003002329.
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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.