FDA inspection
Cutting Edge Products Llc: FDA inspection ending Jun 15, 2016
FDA inspection 973787 · Voluntary Action Indicated (VAI) · Fairport, NY
Key facts
| Inspection ID | 973787 |
|---|---|
| Firm | Cutting Edge Products Llc |
| FEI number | 3004105283 |
| Address | 350 Turk Hill Park |
| City | Fairport |
| State | NY |
| ZIP | 14450 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jun 15, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| 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