GC Rieber VivoMega AS
FDA import alert and refusal historyKristiansund N, NorwayFEI 3009710265
As of October 26, 2026, GC Rieber VivoMega AS has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 10, 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 GC Rieber VivoMega AS
2 records, newest first. Each line links to the FDA page it came from.
Questions about GC Rieber VivoMega AS
- Is GC Rieber VivoMega AS on an FDA import alert?
- No listing for GC Rieber VivoMega AS appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Norway page.
- Has FDA refused shipments from GC Rieber VivoMega AS?
- No FDA import refusals for GC Rieber VivoMega AS appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was GC Rieber VivoMega AS last inspected by FDA?
- FDA's most recent inspection of GC Rieber VivoMega AS with a final classification is dated September 10, 2024 and was classified NAI (No Action Indicated).
- What is GC Rieber VivoMega AS's FEI number?
- GC Rieber VivoMega AS's FDA Establishment Identifier (FEI) is 3009710265.
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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.