FDA Inspection 869719 — Stereo Optical Co Inc

Stereo Optical Co Inc — FEI 1419226

The FDA completed an inspection of Stereo Optical Co Inc on Mar 18, 2014 in Chicago, IL. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 18, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Chicago, IL (United States)

Citations

IDCFRDescription
230221 CFR 820.20(e)Quality System Procedures
63021 CFR 803.17Lack of Written MDR Procedures