FDA inspection
American X-Ray Co Inc: FDA inspection ending Jan 30, 2001
FDA inspection 65015 · No Action Indicated (NAI) · Louisville, TN
Key facts
| Inspection ID | 65015 |
|---|---|
| Firm | American X-Ray Co Inc |
| FEI number | 1049013 |
| Address | 3031 Topside Business Park Drive, P.O. Box 870 |
| City | Louisville |
| State | TN |
| ZIP | 37777-0870 |
| Fiscal year | 2001 |
| Inspection end date | Jan 30, 2001 |
| Classification | No Action Indicated (NAI) |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| Product type | Devices |
At a glance
- None Citations
- None 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