FDA inspection

Molteno Ophthalmic Limited: FDA inspection ending Nov 14, 2019

FDA inspection 1113342 · Voluntary Action Indicated (VAI) · Dunedin

Key facts

Inspection ID 1113342
Firm Molteno Ophthalmic Limited
FEI number 3001227772
Address 152 Frederick Street
City Dunedin
Country New Zealand
Fiscal year 2020
Inspection end date Nov 14, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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