FDA Inspection 620241 — CooperVision Limited

CooperVision Limited — FEI 3002807783

The FDA completed an inspection of CooperVision Limited on Sep 22, 2009 in Eastleigh. 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
Sep 22, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Eastleigh (United Kingdom)

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