FDA inspection

Dynarex Corporation: FDA inspection ending Mar 2, 2017

FDA inspection 1005494 · Voluntary Action Indicated (VAI) · Orangeburg, NY

Key facts

Inspection ID 1005494
Firm Dynarex Corporation
FEI number 2431014
Address 10 Glenshaw St
City Orangeburg
State NY
ZIP 10962
Country United States
Fiscal year 2017
Inspection end date Mar 2, 2017
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
  • 10–99 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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