FDA Inspection 1210674 — International Medical Devices, Inc

International Medical Devices, Inc — FEI 3010606546

The FDA completed an inspection of International Medical Devices, Inc on July 20, 2023 in Beverly Hills, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 20, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Beverly Hills, CA (United States)

Citations

IDCFRDescription
343221 CFR 820.75(b)(2)Documentation of validated process performance
73121 CFR 803.50(a)(1)Report of Death or Serious Injury