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FDA Inspection 1262120 — Molteno Ophthalmic Limited

Molteno Ophthalmic Limited — FEI 3001227772

The FDA completed an inspection of Molteno Ophthalmic Limited on December 18, 2024 in Dunedin. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 18, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Dunedin (New Zealand)

Facility

Other inspections at this facility

  • 1113342 (VAI Thu Nov 14 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 903489 (OAI Thu Oct 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 724115 (VAI Thu Apr 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 634822 (OAI Wed Dec 02 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources