FDA inspection
Camda Corporation DBA KMC International: FDA inspection ending Oct 13, 1999
FDA inspection 749 · No Action Indicated (NAI) · Pasadena, CA
Key facts
| Inspection ID | 749 |
|---|---|
| Firm | Camda Corporation DBA KMC International |
| FEI number | 3000718667 |
| Address | 398 W Washington Blvd |
| City | Pasadena |
| State | CA |
| ZIP | 91103-2000 |
| Fiscal year | 2000 |
| Inspection end date | Oct 13, 1999 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: 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