FDA inspection
Kerma Medical Products, Inc: FDA inspection ending Jul 7, 2017
FDA inspection 1024609 · No Action Indicated (NAI) · Suffolk, VA
Key facts
| Inspection ID | 1024609 |
|---|---|
| Firm | Kerma Medical Products, Inc |
| FEI number | 1000123280 |
| Address | 215 Suburban Dr |
| City | Suffolk |
| State | VA |
| ZIP | 23434 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jul 7, 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
- 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