FDA inspection
EMD Millipore Corporation: FDA inspection ending Dec 14, 2006
FDA inspection 452281 · Voluntary Action Indicated (VAI) · Temecula, CA
Key facts
| Inspection ID | 452281 |
|---|---|
| Firm | EMD Millipore Corporation |
| FEI number | 2024094 |
| Address | 28820 Single Oak Dr |
| City | Temecula |
| State | CA |
| ZIP | 92590-3607 |
| Fiscal year | 2007 |
| Inspection end date | Dec 14, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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