GEI Gruppo Essenziero Italiano S.p.A.
FDA import alert and refusal historySettimo Torinese, ItalyFEI 3010393883
As of October 27, 2026, GEI Gruppo Essenziero Italiano S.p.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on June 27, 2019, most often for color additive unsafe under section 721 (UNSAFE COL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Fluid/dry milk products not elsewhere mentioned, n.e.c. · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for GEI Gruppo Essenziero Italiano S.p.A.
3 records, newest first. Each line links to the FDA page it came from.
2025
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2019
- Import refusalSource
Refused, 2 lines in one entry: Fluid/dry milk products not elsewhere mentioned, n.e.c.UNSAFE COLEntry BJU-1110717-6Show 2 linesHide lines
- Refused, Fluid/dry milk products not elsewhere mentioned, n.e.c.UNSAFE COLEntry BJU-1110717-6Source
- Refused, Fluid/dry milk products not elsewhere mentioned, n.e.c.UNSAFE COLEntry BJU-1110717-6Source
Refusal charges, in plain English
- UNSAFE COL2 refused lines
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about GEI Gruppo Essenziero Italiano S.p.A.
- Is GEI Gruppo Essenziero Italiano S.p.A. on an FDA import alert?
- No listing for GEI Gruppo Essenziero Italiano S.p.A. appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Italy page.
- Has FDA refused shipments from GEI Gruppo Essenziero Italiano S.p.A.?
- Yes. FDA refused 2 shipment lines from GEI Gruppo Essenziero Italiano S.p.A. on June 27, 2019. The most recent, on June 27, 2019, was fluid/dry milk products not elsewhere mentioned, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse GEI Gruppo Essenziero Italiano S.p.A.'s shipments?
- The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 2 lines).
- When was GEI Gruppo Essenziero Italiano S.p.A. last inspected by FDA?
- FDA's most recent inspection of GEI Gruppo Essenziero Italiano S.p.A. with a final classification is dated September 11, 2025 and was classified VAI (Voluntary Action Indicated).
- What is GEI Gruppo Essenziero Italiano S.p.A.'s FEI number?
- GEI Gruppo Essenziero Italiano S.p.A.'s FDA Establishment Identifier (FEI) is 3010393883.
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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.