FDA inspection
Luetje II, Dr Charles M: FDA inspection ending Apr 28, 2000
FDA inspection 21320 · No Action Indicated (NAI) · Kansas City, MO
Key facts
| Inspection ID | 21320 |
|---|---|
| Firm | Luetje II, Dr Charles M |
| FEI number | 3002969997 |
| Address | 4200 Pennsylvania Ave Ste 205, Midwest Ear Institute Inc |
| City | Kansas City |
| State | MO |
| ZIP | 64111-6913 |
| Fiscal year | 2000 |
| Inspection end date | Apr 28, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| 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