FDA Inspection 970313 — Medisca Inc

Medisca Inc — FEI 3008079406

The FDA completed an inspection of Medisca Inc on Jan 15, 2016 in Las Vegas, NV. 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 15, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Las Vegas, NV (United States)

Citations

IDCFRDescription
317221 CFR 820.198(c)Investigation of device failures