FDA inspection

Medikomp Gmbh: FDA inspection ending Oct 20, 2016

FDA inspection 992713 · Voluntary Action Indicated (VAI) · Rastatt

Key facts

Inspection ID 992713
Firm Medikomp Gmbh
FEI number 3007427881
Address Kehler Str. 31
City Rastatt
Fiscal year 2017
Inspection end date Oct 20, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|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
  • 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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