FDA Inspection 1187483 — DX PRODUCTS LIMITED
The FDA completed an inspection of DX PRODUCTS LIMITED on Nov 3, 2022 in Wakefield. 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). 4 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 3, 2022
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wakefield (United Kingdom)
Citations
| ID | CFR | Description |
|---|---|---|
| 14713 | 21 CFR 820.198(a) | Lack of or inadequate complaint procedures |
| 14721 | 21 CFR 820.70(g)(2) | Periodic equipment inspections |
| 3170 | 21 CFR 820.198(b) | Review and evaluation for investigation |
| 479 | 21 CFR 820.50 | Purchasing controls, Lack of or inadequate procedures |