FDA Inspection 1250090 — Clariance-SAS

Clariance-SAS — FEI 3008992889

The FDA completed an inspection of Clariance-SAS on Sep 26, 2024 in Beaurains. 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
Sep 26, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Beaurains (France)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation