FDA inspection

Opgen, Inc.: FDA inspection ending Nov 19, 2015

FDA inspection 954609 · Voluntary Action Indicated (VAI) · Woburn, MA

Key facts

Inspection ID 954609
Firm Opgen, Inc.
FEI number 3004080598
Address 400 Tradecenter Ste 6990
City Woburn
State MA
ZIP 01801
Country United States
Fiscal year 2016
Inspection end date Nov 19, 2015
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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