FDA Inspection 1262120 — Molteno Ophthalmic Limited

Molteno Ophthalmic Limited — FEI 3001227772

The FDA completed an inspection of Molteno Ophthalmic Limited on Dec 18, 2024 in Dunedin. 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
Dec 18, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Dunedin (New Zealand)

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