FDA inspection

Instrumed GmbH: FDA inspection ending Oct 25, 2018

FDA inspection 1074891 · No Action Indicated (NAI) · Tuttlingen

Key facts

Inspection ID 1074891
Firm Instrumed GmbH
FEI number 3007290840
Address Unter Buchsteig 3
City Tuttlingen
Country Germany
Fiscal year 2019
Inspection end date Oct 25, 2018
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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