FDA inspection
HCMI Inc: FDA inspection ending Sep 6, 2002
FDA inspection 237356 · Official Action Indicated (OAI) · Springfield, MO
Key facts
| Inspection ID | 237356 |
|---|---|
| Firm | HCMI Inc |
| FEI number | 1929884 |
| Address | 2146 E Pythian St |
| City | Springfield |
| State | MO |
| ZIP | 65802-2269 |
| Fiscal year | 2002 |
| Inspection end date | Sep 6, 2002 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 10–99 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