FDA Inspection 809759 — Volk Optical Inc

Volk Optical Inc — FEI 1000122772

The FDA completed an inspection of Volk Optical Inc on October 24, 2012 in Mentor, OH. 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
October 24, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Mentor, OH (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures