FDA inspection
Misonix, Inc.: FDA inspection ending May 19, 2017
FDA inspection 1017560 · No Action Indicated (NAI) · Farmingdale, NY
Key facts
| Inspection ID | 1017560 |
|---|---|
| Firm | Misonix, Inc. |
| FEI number | 2435119 |
| Address | 11830 Canon Blvd Ste A |
| City | Farmingdale |
| State | NY |
| ZIP | 11735 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | May 19, 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
- Yes Form FDA 483 issued
- Yes 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