FDA Inspection 972372 — Corning Incorporated Discovery Labware

Corning Incorporated Discovery Labware — FEI 1000110807

The FDA completed an inspection of Corning Incorporated Discovery Labware on May 5, 2016 in Durham, NC. 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
May 5, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Durham, NC (United States)

Citations

IDCFRDescription
230221 CFR 820.20(e)Quality System Procedures