FDA inspection
Air Kinetic Technologies Corp.: FDA inspection ending Feb 25, 2016
FDA inspection 960670 · No Action Indicated (NAI) · Taoyuan
Key facts
| Inspection ID | 960670 |
|---|---|
| Firm | Air Kinetic Technologies Corp. |
| FEI number | 3009307988 |
| Address | No 3 Gongye 5th Rd., Pingzhen Dist. |
| City | Taoyuan |
| Country | Taiwan |
| Fiscal year | 2016 |
| Inspection end date | Feb 25, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data