FDA Inspection 778341 — COVIDIEN FORMERLY MALLINCKRODT DAR S.R.L.

COVIDIEN FORMERLY MALLINCKRODT DAR S.R.L. — FEI 3002808696

The FDA completed an inspection of COVIDIEN FORMERLY MALLINCKRODT DAR S.R.L. on Mar 21, 2012 in Mirandola. 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 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Mirandola (Italy)

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