FDA inspection
Ameriflo2 Incorporated: FDA inspection ending Mar 25, 2016
FDA inspection 980582 · No Action Indicated (NAI) · Indianapolis, IN
Key facts
| Inspection ID | 980582 |
|---|---|
| Firm | Ameriflo2 Incorporated |
| FEI number | 3013744387 |
| Address | 435 Gradle Dr |
| City | Indianapolis |
| State | IN |
| ZIP | 46241 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Mar 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