FDA inspection
Dornier Medtech America, Inc.: FDA inspection ending May 15, 2001
FDA inspection 72165 · Voluntary Action Indicated (VAI) · Kennesaw, GA
Key facts
| Inspection ID | 72165 |
|---|---|
| Firm | Dornier Medtech America, Inc. |
| FEI number | 1037955 |
| Address | 1155 Roberts Blvd NW |
| City | Kennesaw |
| State | GA |
| ZIP | 30144-3600 |
| Fiscal year | 2001 |
| Inspection end date | May 15, 2001 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 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