FDA Inspection 1288238 — Amphenol DC Electronics Inc.
The FDA completed an inspection of Amphenol DC Electronics Inc. on Oct 23, 2025 in San Jose, 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). 3 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 23, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- San Jose, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 14713 | 21 CFR 820.198(a) | Lack of or inadequate complaint procedures |
| 21425 | 21 CFR 820.184(f) | DHR - UDI not included |
| 3118 | 21 CFR 820.75(a) | Documentation |