FDA Inspection 898181 — Ortho Kinetics Corp

Ortho Kinetics Corp — FEI 1000160800

The FDA completed an inspection of Ortho Kinetics Corp on Sep 23, 2014 in Vista, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 23, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Vista, CA (United States)