FDA inspection
Kerma Medical Products, Inc: FDA inspection ending Sep 26, 2006
FDA inspection 446161 · Voluntary Action Indicated (VAI) · Suffolk, VA
Key facts
| Inspection ID | 446161 |
|---|---|
| Firm | Kerma Medical Products, Inc |
| FEI number | 1000123280 |
| Address | 215 Suburban Dr |
| City | Suffolk |
| State | VA |
| ZIP | 23434-2519 |
| Fiscal year | 2006 |
| Inspection end date | Sep 26, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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