FDA Inspection 1244533 — Ortho Kinetics Corp

Ortho Kinetics Corp — FEI 1000160800

The FDA completed an inspection of Ortho Kinetics Corp on Jun 28, 2024 in Vista, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 28, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Vista, CA (United States)