FDA Inspection 953142 — Padtest, LLC
The FDA completed an inspection of Padtest, LLC on Dec 21, 2015 in Scottsdale, AZ. 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
- Dec 21, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Scottsdale, AZ (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 537 | 21 CFR 820.70(a) | Production processes |
| 631 | 21 CFR 803.17(a)(1) | Lack of System for Event Evaluations |
| 632 | 21 CFR 803.17(a)(2) | Lack of System for Determining MDR Events |