FDA inspection

Auxogyn Inc.: FDA inspection ending Jun 1, 2016

FDA inspection 980999 · Voluntary Action Indicated (VAI) · Menlo Park, CA

Key facts

Inspection ID 980999
Firm Auxogyn Inc.
FEI number 3009716149
Address 1490 Obrien Dr Ste A
City Menlo Park
State CA
ZIP 94025
Country United States
Fiscal year 2016
Inspection end date Jun 1, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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