FDA inspection
Klarity Medical Products LLC: FDA inspection ending Feb 25, 2020
FDA inspection 1119795 · Official Action Indicated (OAI) · Heath, OH
Key facts
| Inspection ID | 1119795 |
|---|---|
| Firm | Klarity Medical Products LLC |
| FEI number | 3001236129 |
| Address | 600 Industrial Pkwy |
| City | Heath |
| State | OH |
| ZIP | 43056 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Feb 25, 2020 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 606982 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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