FDA Inspection 821141 — HIQ Solutions Group
The FDA completed an inspection of HIQ Solutions Group on Feb 28, 2013 in Miami, FL. 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
- Feb 28, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Miami, FL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 5907 | 21 CFR 1020.30(d)(1) | Report of assembly submitted within 15 days |