FDA inspection

AcelRx Pharmaceuticals, Inc.: FDA inspection ending Jun 30, 2014

FDA inspection 883185 · Voluntary Action Indicated (VAI) · Hayward, CA

Key facts

Inspection ID 883185
Firm AcelRx Pharmaceuticals, Inc.
FEI number 3006386491
Address 25821 Industrial Blvd Ste 400
City Hayward
State CA
ZIP 94545
Country United States
Fiscal year 2014
Inspection end date Jun 30, 2014
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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