FDA Inspection 658116 — Covidien LP

Covidien LP — FEI 1282497

The FDA completed an inspection of Covidien LP on Jun 14, 2010 in Mansfield, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 14, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Postmarket Surv. and Epidemiology
Location
Mansfield, MA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.