FDA Inspection 1026740 — VectraCor, Inc

VectraCor, Inc — FEI 3009443693

The FDA completed an inspection of VectraCor, Inc on September 27, 2017 in Totowa, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 27, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Totowa, NJ (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation