FDA Inspection 970568 — Ortho Kinetics Corp
The FDA completed an inspection of Ortho Kinetics Corp on Apr 21, 2016 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
- Apr 21, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vista, CA (United States)