FDA Inspection 1227601 — GMV SRL

GMV SRL — FEI 3013551587

The FDA completed an inspection of GMV SRL on Jan 24, 2024 in Rome. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 24, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Rome (Italy)

Citations

IDCFRDescription
327021 CFR 820.80(c)Documentation