FDA Inspection 1316828 — Cadence Device, Inc.
The FDA completed an inspection of Cadence Device, Inc. on May 7, 2026 in Cranberry Township, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- May 7, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cranberry Township, PA (United States)