FDA inspection

Exergen Corporation: FDA inspection ending Jan 19, 2017

FDA inspection 997742 · Voluntary Action Indicated (VAI) · Watertown, MA

Key facts

Inspection ID 997742
Firm Exergen Corporation
FEI number 1221195
Address 400 Pleasant St
City Watertown
State MA
ZIP 02472
Country United States
Fiscal year 2017
Inspection end date Jan 19, 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
  • 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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