FDA inspection
Gyrus ACMI, Inc.: FDA inspection ending Jun 28, 2006
FDA inspection 432795 · Official Action Indicated (OAI) · Redmond, WA
Key facts
| Inspection ID | 432795 |
|---|---|
| Firm | Gyrus ACMI, Inc. |
| FEI number | 3004450998 |
| Address | 6675 185th Ave Ne |
| City | Redmond |
| State | WA |
| ZIP | 98052-5038 |
| Fiscal year | 2006 |
| Inspection end date | Jun 28, 2006 |
| Classification | Official Action Indicated (OAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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