FDA inspection
Kimball Electronics - Indianapolis: FDA inspection ending Oct 16, 2015
FDA inspection 947450 · Official Action Indicated (OAI) · Indianapolis, IN
Key facts
| Inspection ID | 947450 |
|---|---|
| Firm | Kimball Electronics - Indianapolis |
| FEI number | 3004598644 |
| Address | 2950 N Catherwood Ave |
| City | Indianapolis |
| State | IN |
| ZIP | 46219 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Oct 16, 2015 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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