FDA inspection
Eaton Manufacturing Corporation Dba Eaton Medical: FDA inspection ending May 1, 2008
FDA inspection 518845 · Voluntary Action Indicated (VAI) · Memphis, TN
Key facts
| Inspection ID | 518845 |
|---|---|
| Firm | Eaton Manufacturing Corporation Dba Eaton Medical |
| FEI number | 1000113105 |
| Address | 1401 Heistan Pl |
| City | Memphis |
| State | TN |
| ZIP | 38104-4729 |
| Fiscal year | 2008 |
| Inspection end date | May 1, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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