FDA Inspection 1333118 — Kinamed Inc
The FDA completed an inspection of Kinamed Inc on Aug 27, 2026 in Camarillo, 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). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 27, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Camarillo, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 23230 | ISO 13485:2016 Clause 8.2.6 | Monitoring and measurement requirements of product characteristics are not met |