FDA inspection

Instrumed GmbH: FDA inspection ending Jan 29, 2015

FDA inspection 935389 · No Action Indicated (NAI) · Tuttlingen

Key facts

Inspection ID 935389
Firm Instrumed GmbH
FEI number 3007290840
Address Unter Buchsteig 3
City Tuttlingen
Country Germany
Fiscal year 2015
Inspection end date Jan 29, 2015
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

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