FDA Inspection 634822 — Molteno Ophthalmic Limited

Molteno Ophthalmic Limited — FEI 3001227772

The FDA completed an inspection of Molteno Ophthalmic Limited on Dec 2, 2009 in Dunedin. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Dec 2, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Dunedin (New Zealand)

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