FDA Inspection 798394 — VIDAR Systems Corp

VIDAR Systems Corp — FEI 2027116

The FDA completed an inspection of VIDAR Systems Corp on Aug 29, 2012 in Herndon, VA. 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)
End Date
Aug 29, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Herndon, VA (United States)

Citations

IDCFRDescription
407021 CFR 820.30(g)Design validation - documentation