FDA inspection

Morcher Gmbh: FDA inspection ending Jul 10, 2008

FDA inspection 528383 · No Action Indicated (NAI) · Stuttgart

Key facts

Inspection ID 528383
Firm Morcher Gmbh
FEI number 1000447964
Address Kapuzinerweg 12
City Stuttgart
Fiscal year 2008
Inspection end date Jul 10, 2008
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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