FDA inspection
MDF Instruments Direct, Inc.: FDA inspection ending May 3, 2012
FDA inspection 780633 · Voluntary Action Indicated (VAI) · Agoura Hills, CA
Key facts
| Inspection ID | 780633 |
|---|---|
| Firm | MDF Instruments Direct, Inc. |
| FEI number | 3005374305 |
| Address | 5016 Chesebro Rd Ste 100 |
| City | Agoura Hills |
| State | CA |
| ZIP | 91301 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | May 3, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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