FDA Inspection 950878 — Light Sources, Inc.

Light Sources, Inc. — FEI 1221013

The FDA completed an inspection of Light Sources, Inc. on November 17, 2015 in Orange, CT. 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
November 17, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Orange, CT (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures