FDA Inspection 1247685 — MedCAD

MedCAD — FEI 3021635140

The FDA completed an inspection of MedCAD on Jul 1, 2024 in Plano, TX. 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 1, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Plano, TX (United States)