FDA Inspection 634822 — Molteno Ophthalmic Limited
The FDA completed an inspection of Molteno Ophthalmic Limited on December 2, 2009 in Dunedin. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- December 2, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Dunedin (New Zealand)