FDA inspection

Gardner Denver Thomas Inc: FDA inspection ending Aug 3, 2011

FDA inspection 737266 · No Action Indicated (NAI) · Monroe, LA

Key facts

Inspection ID 737266
Firm Gardner Denver Thomas Inc
FEI number 3007725233
Address 4601 Central Ave
City Monroe
State LA
ZIP 71203
Country United States
Fiscal year 2011
Inspection end date Aug 3, 2011
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

Browse all FDA inspections