FDA inspection
Covidien Medical Products (Shanghai) Manufacturing L.L.C.: FDA inspection ending Oct 21, 2010
FDA inspection 697504 · No Action Indicated (NAI) · Shanghai
Key facts
| Inspection ID | 697504 |
|---|---|
| Firm | Covidien Medical Products (Shanghai) Manufacturing L.L.C. |
| FEI number | 3006451981 |
| Address | Building 10 789 Puxinglu, Pujiang, Minhang; Minxing |
| City | Shanghai |
| Country | China |
| Fiscal year | 2011 |
| Inspection end date | Oct 21, 2010 |
| Classification | No Action Indicated (NAI) |
| 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