FDA Inspection 1040485 — Cadence Inc
The FDA completed an inspection of Cadence Inc on Dec 14, 2017 in Staunton, VA. 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
- Dec 14, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Staunton, VA (United States)