FDA Inspection 1074704 — AMPHENOL ALDEN PRODUCTS
The FDA completed an inspection of AMPHENOL ALDEN PRODUCTS on October 25, 2018 in Shenzhen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 25, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)
Citations
| ID | CFR | Description |
|---|---|---|
| 2371 | 21 CFR 820.30(a) | Design control - no procedures |
| 3159 | 21 CFR 820.184 | DHR content |
| 3232 | 21 CFR 820.72(a) | Equipment suitability & capability |
| 3680 | 21 CFR 820.70(a) | Process control procedures, Lack of or inadequate procedures |