FDA Inspection 987004 — Corindus Inc

Corindus Inc — FEI 3007822508

The FDA completed an inspection of Corindus Inc on October 4, 2016 in Waltham, MA. 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 4, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Waltham, MA (United States)

Citations

IDCFRDescription
73221 CFR 803.50(a)(2)Individual Report of Malfunction