FDA Inspection 812526 — Covidien, LP
The FDA completed an inspection of Covidien, LP on December 6, 2012 in North Haven, CT. 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
- December 6, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- North Haven, CT (United States)
Additional Details
Postmarket Audit Inspections