FDA Inspection 651875 — Prestige Medical

Prestige Medical — FEI 2081040

The FDA completed an inspection of Prestige Medical on March 10, 2010 in Northridge, CA. 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
March 10, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Northridge, CA (United States)

Citations

IDCFRDescription
418921 CFR 820.198(a)General