FDA inspection

Gentherman Medical, Llc: FDA inspection ending Aug 25, 2017

FDA inspection 1041699 · Voluntary Action Indicated (VAI) · Blue Ash, OH

Key facts

Inspection ID 1041699
Firm Gentherman Medical, Llc
FEI number 1516825
Address 12011 Mosteller Rd Fl 3
City Blue Ash
State OH
ZIP 45241-1528
Fiscal year 2017
Inspection end date Aug 25, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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