FDA inspection
Medical Instrument Development Laboratories, Inc.: FDA inspection ending Feb 5, 2003
FDA inspection 255315 · Voluntary Action Indicated (VAI) · San Leandro, CA
Key facts
| Inspection ID | 255315 |
|---|---|
| Firm | Medical Instrument Development Laboratories, Inc. |
| FEI number | 1000221463 |
| Address | 557 Mccormick St |
| City | San Leandro |
| State | CA |
| ZIP | 94577-1107 |
| Fiscal year | 2003 |
| Inspection end date | Feb 5, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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