FDA inspection

Gardner Denver Thomas Inc: FDA inspection ending Feb 6, 2015

FDA inspection 913129 · Voluntary Action Indicated (VAI) · Monroe, LA

Key facts

Inspection ID 913129
Firm Gardner Denver Thomas Inc
FEI number 3007725233
Address 4601 Central Ave
City Monroe
State LA
ZIP 71203
Country United States
Fiscal year 2015
Inspection end date Feb 6, 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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