FDA inspection

Gentherm Medical, LLC: FDA inspection ending Mar 1, 2013

FDA inspection 820605 · No Action Indicated (NAI) · Blue Ash, OH

Key facts

Inspection ID 820605
Firm Gentherm Medical, LLC
FEI number 1516825
Address 12011 Mosteller Rd Fl 3
City Blue Ash
State OH
ZIP 45241
Country United States
Fiscal year 2013
Inspection end date Mar 1, 2013
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
  • 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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