FDA Inspection 572319 — Covidien LP
The FDA completed an inspection of Covidien LP on Mar 27, 2009 in Mansfield, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 27, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Mansfield, MA (United States)