FDA Inspection 1198001 — Bien-Air Surgery SA

Bien-Air Surgery SA — FEI 3003800209

The FDA completed an inspection of Bien-Air Surgery SA on February 16, 2023 in Le Noirmont. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 16, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Le Noirmont (Switzerland)

Citations

IDCFRDescription
73221 CFR 803.50(a)(2)Individual Report of Malfunction