FDA inspection
Gyrus ACMI, Inc.: FDA inspection ending Jul 27, 2017
FDA inspection 1020250 · No Action Indicated (NAI) · Brooklyn Park, MN
Key facts
| Inspection ID | 1020250 |
|---|---|
| Firm | Gyrus ACMI, Inc. |
| FEI number | 3011050570 |
| Address | 9600 Louisiana Ave N |
| City | Brooklyn Park |
| State | MN |
| ZIP | 55445 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jul 27, 2017 |
| 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
- 10–99 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