FDA Inspection 745728 — Covidien LP
The FDA completed an inspection of Covidien LP on September 20, 2011 in Mansfield, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 20, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Mansfield, MA (United States)