FDA inspection

MK Medical: FDA inspection ending Jun 28, 2018

FDA inspection 1062702 · No Action Indicated (NAI) · Emmingen-Liptingen

Key facts

Inspection ID 1062702
Firm MK Medical
FEI number 3010673850
Address Jahnstr. 12
City Emmingen-Liptingen
Country Germany
Fiscal year 2018
Inspection end date Jun 28, 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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