FDA inspection

Earlens Corporation: FDA inspection ending Oct 30, 2019

FDA inspection 1121817 · Voluntary Action Indicated (VAI) · Menlo Park, CA

Key facts

Inspection ID 1121817
Firm Earlens Corporation
FEI number 3010863048
Address 4045A Campbell Ave
City Menlo Park
State CA
ZIP 94025-1006
Fiscal year 2020
Inspection end date Oct 30, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical 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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